Syndrome

"Syndrome" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "syndrome"

  • Syndrome - See Also: Disease;
    • 48,XXXX - Q97.1 Female with more than three X chromosomes
    • 49,XXXXX - Q97.1 Female with more than three X chromosomes
    • 5q minus NOS - D46.C Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality
    • abdominal
      • acute - R10.0 Acute abdomen
      • muscle deficiency - Q79.4 Prune belly syndrome
    • abnormal innervation - H02.519 Abnormal innervation syndrome unspecified eye, unspecified eyelid
      • left - H02.516 Abnormal innervation syndrome left eye, unspecified eyelid
        • lower - H02.515 Abnormal innervation syndrome left lower eyelid
        • upper - H02.514 Abnormal innervation syndrome left upper eyelid
      • right - H02.513 Abnormal innervation syndrome right eye, unspecified eyelid
        • lower - H02.512 Abnormal innervation syndrome right lower eyelid
        • upper - H02.511 Abnormal innervation syndrome right upper eyelid
    • abstinence, neonatal - P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction
    • acid pulmonary aspiration, obstetric - O74.0 Aspiration pneumonitis due to anesthesia during labor and delivery
    • acquired immunodeficiency - See: Human, immunodeficiency virus (HIV) disease;
    • activated phosphoinositide 3-kinase delta syndrome [APDS] - D81.82 Activated Phosphoinositide 3-kinase Delta Syndrome [APDS]
    • acute abdominal - R10.0 Acute abdomen
    • acute respiratory distress (adult) (child) - J80 Acute respiratory distress syndrome
      • idiopathic - J84.114 Acute interstitial pneumonitis
    • Adair-Dighton - Q78.0 Osteogenesis imperfecta
    • Adams-Stokes (-Morgagni) - I45.9 Conduction disorder, unspecified
    • adiposogenital - E23.6 Other disorders of pituitary gland
    • adrenal
      • hemorrhage (meningococcal) - A39.1 Waterhouse-Friderichsen syndrome
      • meningococcic - A39.1 Waterhouse-Friderichsen syndrome
    • adrenocortical - See: Cushing's, syndrome;
    • adrenogenital - E25.9 Adrenogenital disorder, unspecified
      • congenital, associated with enzyme deficiency - E25.0 Congenital adrenogenital disorders associated with enzyme deficiency
    • afferent loop NEC - K91.89 Other postprocedural complications and disorders of digestive system
    • Alagille's - Q44.7 Other congenital malformations of liver
    • alcohol withdrawal (without convulsions) - See: Dependence, alcohol, with, withdrawal;
    • Alder's - D72.0 Genetic anomalies of leukocytes
    • Aldrich (-Wiskott) - D82.0 Wiskott-Aldrich syndrome
    • alien hand - R41.4 Neurologic neglect syndrome
    • Alport - Q87.81 Alport syndrome
    • alveolar hypoventilation - E66.2 Morbid (severe) obesity with alveolar hypoventilation
    • alveolocapillary block - J84.10 Pulmonary fibrosis, unspecified
    • amnesic, amnestic (confabulatory) (due to) - See: Disorder, amnesic;
    • amyostatic (Wilson's disease) - E83.01 Wilson's disease
    • androgen insensitivity - E34.50 Androgen insensitivity syndrome, unspecified
      • complete - E34.51 Complete androgen insensitivity syndrome
      • partial - E34.52 Partial androgen insensitivity syndrome
    • androgen resistance - See Also: Syndrome, androgen insensitivity; - E34.50 Androgen insensitivity syndrome, unspecified
    • Angelman - Q93.51 Angelman syndrome
    • anginal - See: Angina;
    • ankyloglossia superior - Q38.1 Ankyloglossia
    • anterior
      • chest wall - R07.89 Other chest pain
      • cord - G83.82 Anterior cord syndrome
      • spinal artery - G95.19 Other vascular myelopathies
        • compression - M47.019 Anterior spinal artery compression syndromes, site unspecified
          • cervical region - M47.012 Anterior spinal artery compression syndromes, cervical region
          • cervicothoracic region - M47.013 Anterior spinal artery compression syndromes, cervicothoracic region
          • lumbar region - M47.016 Anterior spinal artery compression syndromes, lumbar region
          • occipito-atlanto-axial region - M47.011 Anterior spinal artery compression syndromes, occipito-atlanto-axial region
          • thoracic region - M47.014 Anterior spinal artery compression syndromes, thoracic region
          • thoracolumbar region - M47.015 Anterior spinal artery compression syndromes, thoracolumbar region
      • tibial - M76.81 Anterior tibial syndrome
    • antibody deficiency - D80.9 Immunodeficiency with predominantly antibody defects, unspecified
      • agammaglobulinemic - D80.1 Nonfamilial hypogammaglobulinemia
        • hereditary - D80.0 Hereditary hypogammaglobulinemia
      • congenital - D80.0 Hereditary hypogammaglobulinemia
      • hypogammaglobulinemic - D80.1 Nonfamilial hypogammaglobulinemia
        • hereditary - D80.0 Hereditary hypogammaglobulinemia
    • anticardiolipin (-antibody) - D68.61 Antiphospholipid syndrome
    • antidepressant discontinuation - T43.205 Adverse effect of unspecified antidepressants
    • antiphospholipid (-antibody) - D68.61 Antiphospholipid syndrome
    • aortic
      • arch - M31.4 Aortic arch syndrome [Takayasu]
      • bifurcation - I74.09 Other arterial embolism and thrombosis of abdominal aorta
    • aortomesenteric duodenum occlusion - K31.5 Obstruction of duodenum
    • apical ballooning (transient left ventricular) - I51.81 Takotsubo syndrome
    • arcuate ligament - I77.4 Celiac artery compression syndrome
    • argentaffin, argintaffinoma - E34.0 Carcinoid syndrome
    • Arnold-Chiari - See: Arnold-Chiari disease;
    • Arrillaga-Ayerza - I27.0 Primary pulmonary hypertension
    • arterial tortuosity - Q87.82 Arterial tortuosity syndrome
    • arteriovenous steal - T82.898 Other specified complication of vascular prosthetic devices, implants and grafts
    • Asherman's - N85.6 Intrauterine synechiae
    • aspiration, of newborn - See: Aspiration, by substance, with pneumonia;
      • meconium - P24.01 Meconium aspiration with respiratory symptoms
    • ataxia-telangiectasia - G11.3 Cerebellar ataxia with defective DNA repair
    • auriculotemporal - G50.8 Other disorders of trigeminal nerve
    • autoerythrocyte sensitization (Gardner-Diamond) - D69.2 Other nonthrombocytopenic purpura
    • autoimmune lymphoproliferative [ALPS] - D89.82 Autoimmune lymphoproliferative syndrome [ALPS]
    • autoimmune polyglandular - E31.0 Autoimmune polyglandular failure
    • autoinflammatory - M04.9 Autoinflammatory syndrome, unspecified
      • specified type NEC - M04.8 Other autoinflammatory syndromes
    • autosomal - See: Abnormal, autosomes;
    • Avellis' - G46.8 Other vascular syndromes of brain in cerebrovascular diseases
    • Ayerza (-Arrillaga) - I27.0 Primary pulmonary hypertension
    • Babinski-Nageotte - G83.89 Other specified paralytic syndromes
    • Bakwin-Krida - Q78.5 Metaphyseal dysplasia
    • bare lymphocyte - D81.6 Major histocompatibility complex class I deficiency
    • Barré-Guillain - G61.0 Guillain-Barre syndrome
    • Barré-Liéou - M53.0 Cervicocranial syndrome
    • Barrett's - See: Barrett's, esophagus;
    • Barsony-Polgar - K22.4 Dyskinesia of esophagus
    • Barsony-Teschendorf - K22.4 Dyskinesia of esophagus
    • Barth - E78.71 Barth syndrome
    • Bartter's - E26.81 Bartter's syndrome
    • basal cell nevus - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • Basedow's - E05.00 Thyrotoxicosis with diffuse goiter without thyrotoxic crisis or storm
      • with thyroid storm - E05.01 Thyrotoxicosis with diffuse goiter with thyrotoxic crisis or storm
    • basilar artery - G45.0 Vertebro-basilar artery syndrome
    • Batten-Steinert - G71.11 Myotonic muscular dystrophy
    • battered
      • baby or child - See: Maltreatment, child, physical abuse;
      • spouse - See: Maltreatment, adult, physical abuse;
    • Beals - Q87.40 Marfan's syndrome, unspecified
    • Beau's - I51.5 Myocardial degeneration
    • Beck's - I65.8 Occlusion and stenosis of other precerebral arteries
    • Benedikt's - G46.3 Brain stem stroke syndrome
    • Béquez César (-Steinbrinck-Chédiak-Higashi) - E70.330 Chediak-Higashi syndrome
    • Bernhardt-Roth - See: Meralgia paresthetica;
    • Bernheim's - See: Failure, heart, right;
    • big spleen - D73.1 Hypersplenism
    • bilateral polycystic ovarian - E28.2 Polycystic ovarian syndrome
    • Bing-Horton's - See: Horton's headache;
    • Birt-Hogg-Dube syndrome - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • Björck (-Thorsen) - E34.0 Carcinoid syndrome
    • black
      • lung - J60 Coalworker's pneumoconiosis
      • widow spider bite - See: Toxicity, venom, spider, black widow;
    • Blackfan-Diamond - D61.01 Constitutional (pure) red blood cell aplasia
    • Blau - M04.8 Other autoinflammatory syndromes
    • blind loop - K90.2 Blind loop syndrome, not elsewhere classified
      • congenital - Q43.8 Other specified congenital malformations of intestine
      • postsurgical - K91.2 Postsurgical malabsorption, not elsewhere classified
    • blue sclera - Q78.0 Osteogenesis imperfecta
    • blue toe - I75.02 Atheroembolism of lower extremity
    • Boder-Sedgewick - G11.3 Cerebellar ataxia with defective DNA repair
    • Boerhaave's - K22.3 Perforation of esophagus
    • Borjeson Forssman Lehmann - Q89.8 Other specified congenital malformations
    • Bouillaud's - I01.9 Acute rheumatic heart disease, unspecified
    • Bourneville (-Pringle) - Q85.1 Tuberous sclerosis
    • Bouveret (-Hoffman) - I47.9 Paroxysmal tachycardia, unspecified
    • brachial plexus - G54.0 Brachial plexus disorders
    • bradycardia-tachycardia - I49.5 Sick sinus syndrome
    • brain (nonpsychotic) - F09 Unspecified mental disorder due to known physiological condition
      • acute or subacute - See: Delirium;
      • congenital - See: Disability, intellectual;
      • organic - F09 Unspecified mental disorder due to known physiological condition
        • post-traumatic (nonpsychotic) - F07.81 Postconcussional syndrome
          • psychotic - F09 Unspecified mental disorder due to known physiological condition
      • personality change - F07.0 Personality change due to known physiological condition
      • postcontusional - F07.81 Postconcussional syndrome
      • post-traumatic, nonpsychotic - F07.81 Postconcussional syndrome
      • psycho-organic - F09 Unspecified mental disorder due to known physiological condition
      • psychotic - F06.8 Other specified mental disorders due to known physiological condition
      • with psychosis, psychotic reaction - F09 Unspecified mental disorder due to known physiological condition
    • brain stem stroke - G46.3 Brain stem stroke syndrome
    • Brandt's (acrodermatitis enteropathica) - E83.2 Disorders of zinc metabolism
    • broad ligament laceration - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
    • Brock's - J98.11 Atelectasis
    • bronze baby - P83.88 Other specified conditions of integument specific to newborn
    • Brown-Sequard - G83.81 Brown-Sequard syndrome
    • Brugada - I49.8 Other specified cardiac arrhythmias
    • bubbly lung - P27.0 Wilson-Mikity syndrome
    • Buchem's - M85.2 Hyperostosis of skull
    • Budd-Chiari - I82.0 Budd-Chiari syndrome
    • bulbar (progressive) - G12.22 Progressive bulbar palsy
    • Bürger-Grütz - E78.3 Hyperchylomicronemia
    • Burke's - K86.89 Other specified diseases of pancreas
    • Burnett's (milk-alkali) - E83.52 Hypercalcemia
    • burning feet - E53.9 Vitamin B deficiency, unspecified
    • Bywaters' - T79.5 Traumatic anuria
    • Call-Fleming - I67.841 Reversible cerebrovascular vasoconstriction syndrome
    • carbohydrate-deficient glycoprotein (CDGS) - E77.8 Other disorders of glycoprotein metabolism
    • carcinogenic thrombophlebitis - I82.1 Thrombophlebitis migrans
    • carcinoid - E34.0 Carcinoid syndrome
    • cardiac asthma - I50.1 Left ventricular failure, unspecified
    • cardiacos negros - I27.0 Primary pulmonary hypertension
    • cardiofaciocutaneous - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • cardiopulmonary-obesity - E66.2 Morbid (severe) obesity with alveolar hypoventilation
    • cardiorenal - See: Hypertension, cardiorenal;
    • cardiorespiratory distress (idiopathic), newborn - P22.0 Respiratory distress syndrome of newborn
    • cardiovascular renal - See: Hypertension, cardiorenal;
    • carotid
      • artery (hemispheric) (internal) - G45.1 Carotid artery syndrome (hemispheric)
      • body - G90.01 Carotid sinus syncope
      • sinus - G90.01 Carotid sinus syncope
    • carpal tunnel - G56.0 Carpal tunnel syndrome
    • Cassidy (-Scholte) - E34.0 Carcinoid syndrome
    • cat cry - Q93.4 Deletion of short arm of chromosome 5
    • cat eye - Q92.8 Other specified trisomies and partial trisomies of autosomes
    • cauda equina - G83.4 Cauda equina syndrome
    • causalgia - See: Causalgia;
    • celiac - K90.0 Celiac disease
      • artery compression - I77.4 Celiac artery compression syndrome
      • axis - I77.4 Celiac artery compression syndrome
    • central pain - G89.0 Central pain syndrome
    • cerebellar
      • hereditary - G11.9 Hereditary ataxia, unspecified
      • stroke - G46.4 Cerebellar stroke syndrome
    • cerebellomedullary malformation - See: Spina bifida;
    • cerebral
      • artery
        • anterior - G46.1 Anterior cerebral artery syndrome
        • middle - G46.0 Middle cerebral artery syndrome
        • posterior - G46.2 Posterior cerebral artery syndrome
      • gigantism - E22.0 Acromegaly and pituitary gigantism
    • cervical (root) - M53.1 Cervicobrachial syndrome
      • disc - See: Disorder, disc, cervical, with neuritis;
      • fusion - Q76.1 Klippel-Feil syndrome
      • posterior, sympathicus - M53.0 Cervicocranial syndrome
      • rib - Q76.5 Cervical rib
      • sympathetic paralysis - G90.2 Horner's syndrome
    • cervicobrachial (diffuse) - M53.1 Cervicobrachial syndrome
    • cervicocranial - M53.0 Cervicocranial syndrome
    • cervicodorsal outlet - G54.2 Cervical root disorders, not elsewhere classified
    • cervicothoracic outlet - G54.0 Brachial plexus disorders
    • Céstan (-Raymond) - I65.8 Occlusion and stenosis of other precerebral arteries
    • Charcot's (angina cruris) (intermittent claudication) - I73.9 Peripheral vascular disease, unspecified
    • Charcot-Weiss-Baker - G90.09 Other idiopathic peripheral autonomic neuropathy
    • CHARGE - Q89.8 Other specified congenital malformations
    • Chédiak-Higashi (-Steinbrinck) - E70.330 Chediak-Higashi syndrome
    • chest wall - R07.1 Chest pain on breathing
    • Chiari's (hepatic vein thrombosis) - I82.0 Budd-Chiari syndrome
    • Chilaiditi's - Q43.3 Congenital malformations of intestinal fixation
    • child maltreatment - See: Maltreatment, child;
    • chondrocostal junction - M94.0 Chondrocostal junction syndrome [Tietze]
    • chondroectodermal dysplasia - Q77.6 Chondroectodermal dysplasia
    • chromosome 4 short arm deletion - Q93.3 Deletion of short arm of chromosome 4
    • chromosome 5 short arm deletion - Q93.4 Deletion of short arm of chromosome 5
    • chronic
      • infantile neurological, cutaneous and articular (CINCA) - M04.2 Cryopyrin-associated periodic syndromes
      • pain - G89.4 Chronic pain syndrome
        • personality - F68.8 Other specified disorders of adult personality and behavior
    • Churg-Strauss - M30.1 Polyarteritis with lung involvement [Churg-Strauss]
    • Clarke-Hadfield - K86.89 Other specified diseases of pancreas
    • Clerambault's automatism - G93.89 Other specified disorders of brain
    • Clouston's (hidrotic ectodermal dysplasia) - Q82.4 Ectodermal dysplasia (anhidrotic)
    • clumsiness, clumsy child - F82 Specific developmental disorder of motor function
    • cluster headache - G44.009 Cluster headache syndrome, unspecified, not intractable
      • intractable - G44.001 Cluster headache syndrome, unspecified, intractable
      • not intractable - G44.009 Cluster headache syndrome, unspecified, not intractable
    • Coffin-Lowry - Q89.8 Other specified congenital malformations
    • cold injury (newborn) - P80.0 Cold injury syndrome
    • combined immunity deficiency - D81.9 Combined immunodeficiency, unspecified
    • compartment (deep) (posterior) (traumatic) - T79.A0 Compartment syndrome, unspecified
      • abdomen - T79.A3 Traumatic compartment syndrome of abdomen
      • lower extremity (hip, buttock, thigh, leg, foot, toes) - T79.A2 Traumatic compartment syndrome of lower extremity
      • nontraumatic
        • abdomen - M79.A3 Nontraumatic compartment syndrome of abdomen
        • lower extremity (hip, buttock, thigh, leg, foot, toes) - M79.A2 Nontraumatic compartment syndrome of lower extremity
        • specified site NEC - M79.A9 Nontraumatic compartment syndrome of other sites
        • upper extremity (shoulder, arm, forearm, wrist, hand, fingers) - M79.A1 Nontraumatic compartment syndrome of upper extremity
      • postprocedural - See: Syndrome, compartment, nontraumatic;
      • specified site NEC - T79.A9 Traumatic compartment syndrome of other sites
      • upper extremity (shoulder, arm, forearm, wrist, hand, fingers) - T79.A1 Traumatic compartment syndrome of upper extremity
    • complex regional pain - See: Syndrome, pain, complex regional;
    • compression - T79.5 Traumatic anuria
      • anterior spinal - See: Syndrome, anterior, spinal artery, compression;
      • cauda equina - G83.4 Cauda equina syndrome
      • celiac artery - I77.4 Celiac artery compression syndrome
      • vertebral artery - M47.029 Vertebral artery compression syndromes, site unspecified
        • cervical region - M47.022 Vertebral artery compression syndromes, cervical region
        • occipito-atlanto-axial region - M47.021 Vertebral artery compression syndromes, occipito-atlanto-axial region
    • concussion - F07.81 Postconcussional syndrome
    • congenital
      • affecting multiple systems NEC - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
      • central alveolar hypoventilation - G47.35 Congenital central alveolar hypoventilation syndrome
      • facial diplegia - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
      • muscular hypertrophy-cerebral - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
      • oculo-auriculovertebral - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
      • oculofacial diplegia (Moebius) - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
      • rubella (manifest) - P35.0 Congenital rubella syndrome
    • congestion-fibrosis (pelvic), female - N94.89 Other specified conditions associated with female genital organs and menstrual cycle
    • congestive dysmenorrhea - N94.6 Dysmenorrhea, unspecified
    • connective tissue - M35.9 Systemic involvement of connective tissue, unspecified
      • overlap NEC - M35.1 Other overlap syndromes
    • Conn's - E26.01 Conn's syndrome
    • conus medullaris - G95.81 Conus medullaris syndrome
    • cord
      • anterior - G83.82 Anterior cord syndrome
      • posterior - G83.83 Posterior cord syndrome
    • coronary
      • acute NEC - I24.9 Acute ischemic heart disease, unspecified
      • insufficiency or intermediate - I20.0 Unstable angina
      • slow flow - I20.8 Other forms of angina pectoris
    • Costen's (complex) - M26.69 Other specified disorders of temporomandibular joint
    • costochondral junction - M94.0 Chondrocostal junction syndrome [Tietze]
    • costoclavicular - G54.0 Brachial plexus disorders
    • costovertebral - E22.0 Acromegaly and pituitary gigantism
    • Cowden
      • specified NEC - Q85.82 Other Cowden syndrome
    • craniovertebral - M53.0 Cervicocranial syndrome
    • Creutzfeldt-Jakob - See: Creutzfeldt-Jakob disease or syndrome;
    • crib death - R99 Ill-defined and unknown cause of mortality
    • cricopharyngeal - See: Dysphagia;
    • cri-du-chat - Q93.4 Deletion of short arm of chromosome 5
    • croup - J05.0 Acute obstructive laryngitis [croup]
    • CRPS I - See: Syndrome, pain, complex regional I;
    • crush - T79.5 Traumatic anuria
    • cryopyrin-associated periodic - M04.2 Cryopyrin-associated periodic syndromes
    • cryptophthalmos - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • cubital tunnel - See: Lesion, nerve, ulnar;
    • Curschmann (-Batten) (-Steinert) - G71.11 Myotonic muscular dystrophy
    • Cushing's - E24.9 Cushing's syndrome, unspecified
      • alcohol-induced - E24.4 Alcohol-induced pseudo-Cushing's syndrome
      • drug-induced - E24.2 Drug-induced Cushing's syndrome
      • due to
        • alcohol
        • drugs - E24.2 Drug-induced Cushing's syndrome
        • ectopic ACTH - E24.3 Ectopic ACTH syndrome
        • overproduction of pituitary ACTH - E24.0 Pituitary-dependent Cushing's disease
      • overdose or wrong substance given or taken - See: Table of Drugs and Chemicals, by drug, poisoning;
      • pituitary-dependent - E24.0 Pituitary-dependent Cushing's disease
      • specified type NEC - E24.8 Other Cushing's syndrome
    • cystic duct stump - K91.5 Postcholecystectomy syndrome
    • cytokine release - D89.839 Cytokine release syndrome, grade unspecified
      • grade 1 - D89.831 Cytokine release syndrome, grade 1
      • grade 2 - D89.832 Cytokine release syndrome, grade 2
      • grade 3 - D89.833 Cytokine release syndrome, grade 3
      • grade 4 - D89.834 Cytokine release syndrome, grade 4
      • grade 5 - D89.835 Cytokine release syndrome, grade 5
    • Dana-Putnam - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • Danbolt (-Cross) (acrodermatitis enteropathica) - E83.2 Disorders of zinc metabolism
    • Dandy-Walker - Q03.1 Atresia of foramina of Magendie and Luschka
      • with spina bifida - Q07.01 Arnold-Chiari syndrome with spina bifida
    • Danlos' - See Also: Syndrome, Ehlers-Danlos; - Q79.60 Ehlers-Danlos syndrome, unspecified
    • De Quervain - E34.51 Complete androgen insensitivity syndrome
    • de Toni-Fanconi (-Debré) - E72.09 Other disorders of amino-acid transport
      • with cystinosis - E72.04 Cystinosis
    • de Vivo syndrome - E74.810 Glucose transporter protein type 1 deficiency
    • defibrination - See Also: Fibrinolysis;
      • newborn - P60 Disseminated intravascular coagulation of newborn
      • postpartum - O72.3 Postpartum coagulation defects
      • with
        • antepartum hemorrhage - See: Hemorrhage, antepartum, with coagulation defect;
        • intrapartum hemorrhage - See: Hemorrhage, complicating, delivery;
    • Degos' - I77.89 Other specified disorders of arteries and arterioles
    • Déjérine-Roussy - G89.0 Central pain syndrome
    • delayed sleep phase - G47.21 Circadian rhythm sleep disorder, delayed sleep phase type
    • demyelinating - G37.9 Demyelinating disease of central nervous system, unspecified
    • dependence - See: F10-F19 with fourth character .2;
    • depersonalization (-derealization) - F48.1 Depersonalization-derealization syndrome
    • di George's - D82.1 Di George's syndrome
    • diabetes mellitus in newborn infant - P70.2 Neonatal diabetes mellitus
    • diabetes mellitus-hypertension-nephrosis - See: Diabetes, nephrosis;
    • diabetes-nephrosis - See: Diabetes, nephrosis;
    • diabetic amyotrophy - See: Diabetes, amyotrophy;
    • dialysis associated steal - T82.898 Other specified complication of vascular prosthetic devices, implants and grafts
    • Diamond-Blackfan - D61.01 Constitutional (pure) red blood cell aplasia
    • Diamond-Gardener - D69.2 Other nonthrombocytopenic purpura
    • DIC (diffuse or disseminated intravascular coagulopathy) - D65 Disseminated intravascular coagulation [defibrination syndrome]
    • Dighton's - Q78.0 Osteogenesis imperfecta
    • disequilibrium - E87.8 Other disorders of electrolyte and fluid balance, not elsewhere classified
    • Döhle body-panmyelopathic - D72.0 Genetic anomalies of leukocytes
    • dorsolateral medullary - G46.4 Cerebellar stroke syndrome
    • double athetosis - G80.3 Athetoid cerebral palsy
    • Down - See Also: Down syndrome; - Q90.9 Down syndrome, unspecified
    • Dravet (intractable) - G40.834 Dravet syndrome, intractable, without status epilepticus
      • with status epilepticus - G40.833 Dravet syndrome, intractable, with status epilepticus
      • without status epilepticus - G40.834 Dravet syndrome, intractable, without status epilepticus
    • Dresbach's (elliptocytosis) - D58.1 Hereditary elliptocytosis
    • DRESS (drug rash with eosinophilia and systemic symptoms) - D72.12 Drug rash with eosinophilia and systemic symptoms syndrome
    • Dressler's (postmyocardial infarction) - I24.1 Dressler's syndrome
      • postcardiotomy - I97.0 Postcardiotomy syndrome
    • drug rash with eosinophilia and systemic symptoms (DRESS) - D72.12 Drug rash with eosinophilia and systemic symptoms syndrome
    • drug withdrawal, infant of dependent mother - P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction
    • dry eye - H04.12 Dry eye syndrome
    • due to abnormality
      • chromosomal - Q99.9 Chromosomal abnormality, unspecified
        • sex
          • female phenotype - Q97.9 Sex chromosome abnormality, female phenotype, unspecified
          • male phenotype - Q98.9 Sex chromosome abnormality, male phenotype, unspecified
        • specified NEC - Q99.8 Other specified chromosome abnormalities
    • dumping (postgastrectomy) - K91.1 Postgastric surgery syndromes
      • nonsurgical - K31.89 Other diseases of stomach and duodenum
    • Dupré's (meningism) - R29.1 Meningismus
    • dysmetabolic X - E88.81 Metabolic syndrome
    • dyspraxia, developmental - F82 Specific developmental disorder of motor function
    • Eagle-Barrett - Q79.4 Prune belly syndrome
    • Eaton-Lambert - See: Syndrome, Lambert-Eaton;
    • Ebstein's - Q22.5 Ebstein's anomaly
    • ectopic ACTH - E24.3 Ectopic ACTH syndrome
    • eczema-thrombocytopenia - D82.0 Wiskott-Aldrich syndrome
    • Eddowes' - Q78.0 Osteogenesis imperfecta
    • effort (psychogenic) - F45.8 Other somatoform disorders
    • Ehlers-Danlos - Q79.60 Ehlers-Danlos syndrome, unspecified
      • classical (cEDS) (classical EDS) - Q79.61 Classical Ehlers-Danlos syndrome
      • hypermobile (hEDS) (hypermobile EDS) - Q79.62 Hypermobile Ehlers-Danlos syndrome
      • specified NEC - Q79.69 Other Ehlers-Danlos syndromes
      • vascular (vascular EDS) (vEDS) - Q79.63 Vascular Ehlers-Danlos syndrome
    • Eisenmenger's - I27.83 Eisenmenger's syndrome
    • Ekman's - Q78.0 Osteogenesis imperfecta
    • electric feet - E53.8 Deficiency of other specified B group vitamins
    • Ellis-van Creveld - Q77.6 Chondroectodermal dysplasia
    • empty nest - Z60.0 Problems of adjustment to life-cycle transitions
    • endocrine-hypertensive - E27.0 Other adrenocortical overactivity
    • entrapment - See: Neuropathy, entrapment;
    • eosinophilia-myalgia - M35.89 Other specified systemic involvement of connective tissue
    • epileptic - See Also: Epilepsy, by type;
      • absence - G40.A09 Absence epileptic syndrome, not intractable, without status epilepticus
        • intractable - G40.A19 Absence epileptic syndrome, intractable, without status epilepticus
          • with status epilepticus - G40.A11 Absence epileptic syndrome, intractable, with status epilepticus
          • without status epilepticus - G40.A19 Absence epileptic syndrome, intractable, without status epilepticus
        • not intractable - G40.A09 Absence epileptic syndrome, not intractable, without status epilepticus
          • with status epilepticus - G40.A01 Absence epileptic syndrome, not intractable, with status epilepticus
          • without status epilepticus - G40.A09 Absence epileptic syndrome, not intractable, without status epilepticus
    • Erdheim-Chester (ECD) - E88.89 Other specified metabolic disorders
    • Erdheim's - E22.0 Acromegaly and pituitary gigantism
    • erythrocyte fragmentation - D59.4 Other nonautoimmune hemolytic anemias
    • Evans - D69.41 Evans syndrome
    • exhaustion - F48.8 Other specified nonpsychotic mental disorders
    • extrapyramidal - G25.9 Extrapyramidal and movement disorder, unspecified
      • specified NEC - G25.89 Other specified extrapyramidal and movement disorders
    • eye retraction - See: Strabismus;
    • eyelid-malar-mandible - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • Faber's - D50.9 Iron deficiency anemia, unspecified
    • facet - M47.89 Other spondylosis
    • facet joint - See Also: Spondylosis; - M47.819 Spondylosis without myelopathy or radiculopathy, site unspecified
    • facial pain, paroxysmal - G50.0 Trigeminal neuralgia
    • Fallot's - Q21.3 Tetralogy of Fallot
    • familial cold autoinflammatory - M04.2 Cryopyrin-associated periodic syndromes
    • familial eczema-thrombocytopenia (Wiskott-Aldrich) - D82.0 Wiskott-Aldrich syndrome
    • Fanconi (-de Toni) (-Debré) - E72.09 Other disorders of amino-acid transport
      • with cystinosis - E72.04 Cystinosis
    • Fanconi's (anemia) (congenital pancytopenia) - D61.09 Other constitutional aplastic anemia
    • fatigue
      • chronic - G93.32 Myalgic encephalomyelitis/chronic fatigue syndrome
      • postviral - G93.31 Postviral fatigue syndrome
      • psychogenic - F48.8 Other specified nonpsychotic mental disorders
    • faulty bowel habit - K59.39 Other megacolon
    • Feil-Klippel (brevicollis) - Q76.1 Klippel-Feil syndrome
    • Felty's - See: Felty's syndrome;
    • fertile eunuch - E23.0 Hypopituitarism
    • fetal
      • alcohol (dysmorphic) - Q86.0 Fetal alcohol syndrome (dysmorphic)
      • hydantoin - Q86.1 Fetal hydantoin syndrome
    • Fiedler's - I40.1 Isolated myocarditis
    • first arch - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • fish odor - E72.89 Other specified disorders of amino-acid metabolism
    • Fisher's - G61.0 Guillain-Barre syndrome
    • Fitzhugh-Curtis
      • due to
        • Chlamydia trachomatis - A74.81 Chlamydial peritonitis
        • Neisseria gonorrhorea (gonococcal peritonitis) - A54.85 Gonococcal peritonitis
    • Fitz's - See Also: Pancreatitis, acute; - K85.80 Other acute pancreatitis without necrosis or infection
    • Flajani (-Basedow) - E05.00 Thyrotoxicosis with diffuse goiter without thyrotoxic crisis or storm
      • with thyroid storm - E05.01 Thyrotoxicosis with diffuse goiter with thyrotoxic crisis or storm
    • flatback - See: Flatback syndrome;
    • floppy
      • baby - P94.2 Congenital hypotonia
      • iris (intraoeprative) (IFIS) - H21.81 Floppy iris syndrome
      • mitral valve - I34.1 Nonrheumatic mitral (valve) prolapse
    • flush - E34.0 Carcinoid syndrome
    • Foix-Alajouanine - G95.19 Other vascular myelopathies
    • Fong's - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • food protein-induced enterocolitis (FPIES) - K52.21 Food protein-induced enterocolitis syndrome
    • foramen magnum - G93.5 Compression of brain
    • Foster-Kennedy - H47.14 Foster-Kennedy syndrome
    • Foville's (peduncular) - G46.3 Brain stem stroke syndrome
    • fragile X - Q99.2 Fragile X chromosome
    • Franceschetti - Q75.4 Mandibulofacial dysostosis
    • Frey's
      • auriculotemporal - G50.8 Other disorders of trigeminal nerve
      • hyperhidrosis - L74.52 Secondary focal hyperhidrosis
    • Friderichsen-Waterhouse - A39.1 Waterhouse-Friderichsen syndrome
    • Froin's - G95.89 Other specified diseases of spinal cord
    • frontal lobe - F07.0 Personality change due to known physiological condition
    • Fukuhara - E88.49 Other mitochondrial metabolism disorders
    • functional
      • bowel - K59.9 Functional intestinal disorder, unspecified
      • prepubertal castrate - E29.1 Testicular hypofunction
    • Gaisböck's - D75.1 Secondary polycythemia
    • ganglion (basal ganglia brain) - G25.9 Extrapyramidal and movement disorder, unspecified
      • geniculi - G51.1 Geniculate ganglionitis
    • Gardner-Diamond - D69.2 Other nonthrombocytopenic purpura
    • gastroesophageal
      • junction - K22.0 Achalasia of cardia
      • laceration-hemorrhage - K22.6 Gastro-esophageal laceration-hemorrhage syndrome
    • gastrojejunal loop obstruction - K91.89 Other postprocedural complications and disorders of digestive system
    • Gee-Herter-Heubner - K90.0 Celiac disease
    • Gelineau's - G47.419 Narcolepsy without cataplexy
      • with cataplexy - G47.411 Narcolepsy with cataplexy
    • genito-anorectal - A55 Chlamydial lymphogranuloma (venereum)
    • Gerstmann-Sträussler-Scheinker (GSS) - A81.82 Gerstmann-Straussler-Scheinker syndrome
    • Gianotti-Crosti - L44.4 Infantile papular acrodermatitis [Gianotti-Crosti]
    • giant platelet (Bernard-Soulier) - D69.1 Qualitative platelet defects
    • Gilles de la Tourette's - F95.2 Tourette's disorder
    • Glass - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • Gleich's - D72.118 Other hypereosinophilic syndrome
    • goiter-deafness - E07.1 Dyshormogenetic goiter
    • Goldberg - Q89.8 Other specified congenital malformations
    • Goldberg-Maxwell - E34.51 Complete androgen insensitivity syndrome
    • Good's - D83.8 Other common variable immunodeficiencies
    • Gopalan' (burning feet) - E53.8 Deficiency of other specified B group vitamins
    • Gorlin's - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • Gougerot-Blum - L81.7 Pigmented purpuric dermatosis
    • Gouley's - I31.1 Chronic constrictive pericarditis
    • Gower's - R55 Syncope and collapse
    • gray or grey (newborn) - P93.0 Grey baby syndrome
      • platelet - D69.1 Qualitative platelet defects
    • Gubler-Millard - G46.3 Brain stem stroke syndrome
    • Guillain-Barré (-Strohl) - G61.0 Guillain-Barre syndrome
    • gustatory sweating - G50.8 Other disorders of trigeminal nerve
    • Hadfield-Clarke - K86.89 Other specified diseases of pancreas
    • hair tourniquet - See: Constriction, external, by site;
    • Hamman's - J98.19 Other pulmonary collapse
    • hand-foot - L27.1 Localized skin eruption due to drugs and medicaments taken internally
    • hand-shoulder - G90.8 Other disorders of autonomic nervous system
    • hantavirus (cardio)-pulmonary (HPS) (HCPS) - B33.4 Hantavirus (cardio)-pulmonary syndrome [HPS] [HCPS]
    • happy puppet - Q93.51 Angelman syndrome
    • Harada's - H30.81 Harada's disease
    • Hayem-Faber - D50.9 Iron deficiency anemia, unspecified
    • headache NEC - G44.89 Other headache syndrome
      • complicated NEC - G44.59 Other complicated headache syndrome
    • Heberden's - I20.8 Other forms of angina pectoris
    • Hedinger's - E34.0 Carcinoid syndrome
    • Hegglin's - D72.0 Genetic anomalies of leukocytes
    • HELLP (hemolysis, elevated liver enzymes and low platelet count) - O14.2 HELLP syndrome
      • complicating
        • childbirth - O14.24 HELLP syndrome, complicating childbirth
        • puerperium - O14.25 HELLP syndrome, complicating the puerperium
    • hemolytic-uremic - D59.30 Hemolytic-uremic syndrome, unspecified
      • atypical - D59.39 Other hemolytic-uremic syndrome
        • genetic - D59.32 Hereditary hemolytic-uremic syndrome
        • hereditary - D59.32 Hereditary hemolytic-uremic syndrome
        • infection-associated - D59.31 Infection-associated hemolytic-uremic syndrome
        • secondary - D59.39 Other hemolytic-uremic syndrome
        • specified NEC - D59.39 Other hemolytic-uremic syndrome
      • due to genetic disorder - D59.32 Hereditary hemolytic-uremic syndrome
      • familial - D59.32 Hereditary hemolytic-uremic syndrome
      • hereditary - D59.32 Hereditary hemolytic-uremic syndrome
      • infection-associated - D59.31 Infection-associated hemolytic-uremic syndrome
      • secondary - D59.39 Other hemolytic-uremic syndrome
      • specified NEC - D59.39 Other hemolytic-uremic syndrome
      • typical - D59.31 Infection-associated hemolytic-uremic syndrome
    • hemophagocytic, infection-associated - D76.2 Hemophagocytic syndrome, infection-associated
    • Henoch-Schönlein - D69.0 Allergic purpura
    • hepatic flexure - K59.89 Other specified functional intestinal disorders
    • hepatopulmonary - K76.81 Hepatopulmonary syndrome
    • hepatorenal - K76.7 Hepatorenal syndrome
      • following delivery - O90.4 Postpartum acute kidney failure
      • postoperative or postprocedural - K91.83 Postprocedural hepatorenal syndrome
      • postpartum, puerperal - O90.4 Postpartum acute kidney failure
    • hepatourologic - K76.7 Hepatorenal syndrome
    • hereditary alpha tryptasemia - D89.44 Hereditary alpha tryptasemia
    • Herter (-Gee) (nontropical sprue) - K90.0 Celiac disease
    • Heubner-Herter - K90.0 Celiac disease
    • Heyd's - K76.7 Hepatorenal syndrome
    • Hilger's - G90.09 Other idiopathic peripheral autonomic neuropathy
    • histamine-like (fish poisoning) - See: Poisoning, fish;
    • histiocytic - D76.3 Other histiocytosis syndromes
    • histiocytosis NEC - D76.3 Other histiocytosis syndromes
    • HIV infection, acute - B20 Human immunodeficiency virus [HIV] disease
    • Hoffmann-Werdnig - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
    • Hollander-Simons - E88.1 Lipodystrophy, not elsewhere classified
    • Hoppe-Goldflam - G70.00 Myasthenia gravis without (acute) exacerbation
      • in crisis - G70.01 Myasthenia gravis with (acute) exacerbation
      • with exacerbation (acute) - G70.01 Myasthenia gravis with (acute) exacerbation
    • Horner's - G90.2 Horner's syndrome
    • hungry bone - E83.81 Hungry bone syndrome
    • hunterian glossitis - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • Hutchinson's triad - A50.53 Hutchinson's triad
    • hyperabduction - G54.0 Brachial plexus disorders
    • hyperammonemia-hyperornithinemia-homocitrullinemia - E72.4 Disorders of ornithine metabolism
    • hypereosinophilic (HES) - D72.119 Hypereosinophilic syndrome [HES], unspecified
      • idiopathic (IHES) - D72.110 Idiopathic hypereosinophilic syndrome [IHES]
      • lymphocytic variant (LHES) - D72.111 Lymphocytic Variant Hypereosinophilic Syndrome [LHES]
      • myeloid - D72.118 Other hypereosinophilic syndrome
      • specified NEC - D72.118 Other hypereosinophilic syndrome
    • hyperimmunoglobulin D - M04.1 Periodic fever syndromes
    • hyperimmunoglobulin E (IgE) - D82.4 Hyperimmunoglobulin E [IgE] syndrome
    • hyperkalemic - E87.5 Hyperkalemia
    • hyperkinetic - See: Hyperkinesia;
    • hypermobility - M35.7 Hypermobility syndrome
    • hypernatremia - E87.0 Hyperosmolality and hypernatremia
    • hyperosmolarity - E87.0 Hyperosmolality and hypernatremia
    • hyperperfusion - G97.82 Other postprocedural complications and disorders of nervous system
    • hypersplenic - D73.1 Hypersplenism
    • hypertransfusion, newborn - P61.1 Polycythemia neonatorum
    • hyperventilation - F45.8 Other somatoform disorders
    • hyperviscosity ( of serum)
      • polycythemic - D75.1 Secondary polycythemia
      • sclerothymic - D58.8 Other specified hereditary hemolytic anemias
    • hypoglycemic (familial) (neonatal) - E16.2 Hypoglycemia, unspecified
    • hypokalemic - E87.6 Hypokalemia
    • hyponatremic - E87.1 Hypo-osmolality and hyponatremia
    • hypopituitarism - E23.0 Hypopituitarism
    • hypoplastic left-heart - Q23.4 Hypoplastic left heart syndrome
    • hypopotassemia - E87.6 Hypokalemia
    • hyposmolality - E87.1 Hypo-osmolality and hyponatremia
    • hypotension, maternal - O26.5 Maternal hypotension syndrome
    • hypothenar hammer - I73.89 Other specified peripheral vascular diseases
    • hypoventilation, obesity (OHS) - E66.2 Morbid (severe) obesity with alveolar hypoventilation
    • ICF (intravascular coagulation-fibrinolysis) - D65 Disseminated intravascular coagulation [defibrination syndrome]
    • idiopathic
      • cardiorespiratory distress, newborn - P22.0 Respiratory distress syndrome of newborn
      • nephrotic (infantile) - N04.9 Nephrotic syndrome with unspecified morphologic changes
    • iliotibial band - M76.3 Iliotibial band syndrome
    • immobility, immobilization (paraplegic) - M62.3 Immobility syndrome (paraplegic)
    • immune effector cell-associated neurotoxicity (ICANS) - G92.00 Immune effector cell-associated neurotoxicity syndrome, grade unspecified
      • grade
        • 1 - G92.01 Immune effector cell-associated neurotoxicity syndrome, grade 1
        • 2 - G92.02 Immune effector cell-associated neurotoxicity syndrome, grade 2
        • 3 - G92.03 Immune effector cell-associated neurotoxicity syndrome, grade 3
        • 4 - G92.04 Immune effector cell-associated neurotoxicity syndrome, grade 4
        • 5 - G92.05 Immune effector cell-associated neurotoxicity syndrome, grade 5
        • unspecified - G92.00 Immune effector cell-associated neurotoxicity syndrome, grade unspecified
    • immune reconstitution - D89.3 Immune reconstitution syndrome
    • immune reconstitution inflammatory [IRIS] - D89.3 Immune reconstitution syndrome
    • immunity deficiency, combined - D81.9 Combined immunodeficiency, unspecified
    • immunodeficiency
      • acquired - See: Human, immunodeficiency virus (HIV) disease;
      • combined - D81.9 Combined immunodeficiency, unspecified
    • impending coronary - I20.0 Unstable angina
    • impingement, shoulder - M75.4 Impingement syndrome of shoulder
    • inappropriate secretion of antidiuretic hormone - E22.2 Syndrome of inappropriate secretion of antidiuretic hormone
    • infant
      • gestational diabetes - P70.0 Syndrome of infant of mother with gestational diabetes
      • of diabetic mother - P70.1 Syndrome of infant of a diabetic mother
    • infantilism (pituitary) - E23.0 Hypopituitarism
    • inferior vena cava - I87.1 Compression of vein
    • inspissated bile (newborn) - P59.1 Inspissated bile syndrome
    • institutional (childhood) - F94.2 Disinhibited attachment disorder of childhood
    • insufficient sleep - F51.12 Insufficient sleep syndrome
    • intermediate coronary (artery) - I20.0 Unstable angina
    • interspinous ligament - See: Spondylopathy, specified NEC;
    • intestinal
      • carcinoid - E34.0 Carcinoid syndrome
      • knot - K56.2 Volvulus
    • intravascular coagulation-fibrinolysis (ICF) - D65 Disseminated intravascular coagulation [defibrination syndrome]
    • iodine-deficiency, congenital - E00.9 Congenital iodine-deficiency syndrome, unspecified
      • type
        • mixed - E00.2 Congenital iodine-deficiency syndrome, mixed type
        • myxedematous - E00.1 Congenital iodine-deficiency syndrome, myxedematous type
        • neurological - E00.0 Congenital iodine-deficiency syndrome, neurological type
    • IRDS (idiopathic respiratory distress, newborn) - P22.0 Respiratory distress syndrome of newborn
    • irritable
      • bowel - K58.9 Irritable bowel syndrome without diarrhea
        • mixed - K58.2 Mixed irritable bowel syndrome
        • psychogenic - F45.8 Other somatoform disorders
        • specified NEC - K58.8 Other irritable bowel syndrome
        • with
          • constipation - K58.1 Irritable bowel syndrome with constipation
          • diarrhea - K58.0 Irritable bowel syndrome with diarrhea
      • heart (psychogenic) - F45.8 Other somatoform disorders
      • weakness - F48.8 Other specified nonpsychotic mental disorders
    • ischemic
      • bowel (transient) - K55.9 Vascular disorder of intestine, unspecified
        • chronic - K55.1 Chronic vascular disorders of intestine
        • due to mesenteric artery insufficiency - K55.1 Chronic vascular disorders of intestine
      • steal - T82.898 Other specified complication of vascular prosthetic devices, implants and grafts
    • IVC (intravascular coagulopathy) - D65 Disseminated intravascular coagulation [defibrination syndrome]
    • Ivemark's - Q89.01 Asplenia (congenital)
    • Jaccoud's - See: Arthropathy, postrheumatic, chronic;
    • Jackson's - G83.89 Other specified paralytic syndromes
    • Jakob-Creutzfeldt - See: Creutzfeldt-Jakob disease or syndrome;
    • jaw-winking - Q07.8 Other specified congenital malformations of nervous system
    • Jervell-Lange-Nielsen - I45.81 Long QT syndrome
    • jet lag - G47.25 Circadian rhythm sleep disorder, jet lag type
    • Job's - D71 Functional disorders of polymorphonuclear neutrophils
    • Joseph-Diamond-Blackfan - D61.01 Constitutional (pure) red blood cell aplasia
    • jugular foramen - G52.7 Disorders of multiple cranial nerves
    • Kabuki - Q89.8 Other specified congenital malformations
    • Kanner's (autism) - F84.0 Autistic disorder
    • Kartagener's - Q89.3 Situs inversus
    • Kelly's - D50.1 Sideropenic dysphagia
    • Kimmelsteil-Wilson - See: Diabetes, specified type, with Kimmelsteil-Wilson disease;
    • Klein (e)-Levine - G47.13 Recurrent hypersomnia
    • Klippel-Feil (brevicollis) - Q76.1 Klippel-Feil syndrome
    • Köhler-Pellegrini-Steida - See: Bursitis, tibial collateral;
    • König's - K59.89 Other specified functional intestinal disorders
    • Korsakoff (-Wernicke) (nonalcoholic) - F04 Amnestic disorder due to known physiological condition
      • alcoholic - F10.26 Alcohol dependence with alcohol-induced persisting amnestic disorder
    • Kostmann's - D70.0 Congenital agranulocytosis
    • Krabbe's congenital muscle hypoplasia - Q79.8 Other congenital malformations of musculoskeletal system
    • labyrinthine
    • lacunar NEC - G46.7 Other lacunar syndromes
    • Lambert-Eaton - G70.80 Lambert-Eaton syndrome, unspecified
      • in
        • neoplastic disease - G73.1 Lambert-Eaton syndrome in neoplastic disease
        • specified disease NEC - G70.81 Lambert-Eaton syndrome in disease classified elsewhere
    • Landau-Kleffner - See: Epilepsy, specified NEC;
    • Larsen's - Q74.8 Other specified congenital malformations of limb(s)
    • lateral
      • cutaneous nerve of thigh - G57.1 Meralgia paresthetica
      • medullary - G46.4 Cerebellar stroke syndrome
    • Launois' - E22.0 Acromegaly and pituitary gigantism
    • lazy
      • leukocyte - D70.8 Other neutropenia
      • posture - M62.3 Immobility syndrome (paraplegic)
    • Lemiere - I80.8 Phlebitis and thrombophlebitis of other sites
    • Lennox-Gastaut - G40.812 Lennox-Gastaut syndrome, not intractable, without status epilepticus
      • intractable - G40.814 Lennox-Gastaut syndrome, intractable, without status epilepticus
        • with status epilepticus - G40.813 Lennox-Gastaut syndrome, intractable, with status epilepticus
        • without status epilepticus - G40.814 Lennox-Gastaut syndrome, intractable, without status epilepticus
      • not intractable - G40.812 Lennox-Gastaut syndrome, not intractable, without status epilepticus
        • with status epilepticus - G40.811 Lennox-Gastaut syndrome, not intractable, with status epilepticus
        • without status epilepticus - G40.812 Lennox-Gastaut syndrome, not intractable, without status epilepticus
    • lenticular, progressive - E83.01 Wilson's disease
    • Leopold-Levi's - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
    • Lev's - I44.2 Atrioventricular block, complete
    • Lichtheim's - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • Li-Fraumeni - Z15.01 Genetic susceptibility to malignant neoplasm of breast
    • Lightwood's - N25.89 Other disorders resulting from impaired renal tubular function
    • Lignac (de Toni) (-Fanconi) (-Debré) - E72.09 Other disorders of amino-acid transport
      • with cystinosis - E72.04 Cystinosis
    • Likoff's - I20.8 Other forms of angina pectoris
    • limbic epilepsy personality - F07.0 Personality change due to known physiological condition
    • liver-kidney - K76.7 Hepatorenal syndrome
    • lobotomy - F07.0 Personality change due to known physiological condition
    • Löffler's - J82.89 Other pulmonary eosinophilia, not elsewhere classified
    • long arm 18 or 21 deletion - Q93.89 Other deletions from the autosomes
    • long QT - I45.81 Long QT syndrome
    • Louis-Barré - G11.3 Cerebellar ataxia with defective DNA repair
    • low
      • atmospheric pressure - T70.29 Other effects of high altitude
      • back - M54.50 Low back pain, unspecified
      • output (cardiac) - I50.9 Heart failure, unspecified
    • lower radicular, newborn (birth injury) - P14.8 Birth injuries to other parts of peripheral nervous system
    • Luetscher's (dehydration) - E86.0 Dehydration
    • Lupus anticoagulant - D68.62 Lupus anticoagulant syndrome
    • Lutembacher's - Q21.19 Other specified atrial septal defect
    • macrophage activation - D76.1 Hemophagocytic lymphohistiocytosis
      • due to infection - D76.2 Hemophagocytic syndrome, infection-associated
    • magnesium-deficiency - R29.0 Tetany
    • Majeed - M04.8 Other autoinflammatory syndromes
    • Mal de Debarquement - R42 Dizziness and giddiness
    • malabsorption - K90.9 Intestinal malabsorption, unspecified
      • postsurgical - K91.2 Postsurgical malabsorption, not elsewhere classified
    • malformation, congenital, due to
      • alcohol - Q86.0 Fetal alcohol syndrome (dysmorphic)
      • exogenous cause NEC - Q86.8 Other congenital malformation syndromes due to known exogenous causes
      • hydantoin - Q86.1 Fetal hydantoin syndrome
      • warfarin - Q86.2 Dysmorphism due to warfarin
    • malignant
      • carcinoid - E34.0 Carcinoid syndrome
      • neuroleptic - G21.0 Malignant neuroleptic syndrome
    • Mallory-Weiss - K22.6 Gastro-esophageal laceration-hemorrhage syndrome
    • mandibulofacial dysostosis - Q75.4 Mandibulofacial dysostosis
    • manic-depressive - See: Disorder, bipolar;
    • maple-syrup-urine - E71.0 Maple-syrup-urine disease
    • Marable's - I77.4 Celiac artery compression syndrome
    • Marfan's - Q87.40 Marfan's syndrome, unspecified
      • with
        • cardiovascular manifestations - Q87.418 Marfan's syndrome with other cardiovascular manifestations
          • aortic dilation - Q87.410 Marfan's syndrome with aortic dilation
        • ocular manifestations - Q87.42 Marfan's syndrome with ocular manifestations
        • skeletal manifestations - Q87.43 Marfan's syndrome with skeletal manifestation
    • Marie's (acromegaly) - E22.0 Acromegaly and pituitary gigantism
    • mast cell activation - See: Activation, mast cell;
    • maternal hypotension - See: Syndrome, hypotension, maternal;
    • May (-Hegglin) - D72.0 Genetic anomalies of leukocytes
    • McArdle (-Schmidt) (-Pearson) - E74.04 McArdle disease
    • McQuarrie's - E16.2 Hypoglycemia, unspecified
    • meconium plug (newborn) - P76.0 Meconium plug syndrome
    • median arcuate ligament - I77.4 Celiac artery compression syndrome
    • Meekeren-Ehlers-Danlos - Q79.6 Ehlers-Danlos syndromes
    • megavitamin-B6 - E67.2 Megavitamin-B6 syndrome
    • Meige - G24.4 Idiopathic orofacial dystonia
    • MELAS - E88.41 MELAS syndrome
    • Mendelson's - O74.0 Aspiration pneumonitis due to anesthesia during labor and delivery
    • MERRF (myoclonic epilepsy associated with ragged-red fibers) - E88.42 MERRF syndrome
    • mesenteric
      • artery (superior) - K55.1 Chronic vascular disorders of intestine
      • vascular insufficiency - K55.1 Chronic vascular disorders of intestine
    • metabolic - E88.81 Metabolic syndrome
    • metastatic carcinoid - E34.0 Carcinoid syndrome
    • micrognathia-glossoptosis - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • midbrain NEC - G93.89 Other specified disorders of brain
    • middle lobe (lung) - J98.19 Other pulmonary collapse
    • middle radicular - G54.0 Brachial plexus disorders
    • migraine - See Also: Migraine; - G43.909 Migraine, unspecified, not intractable, without status migrainosus
    • Mikulicz' - K11.8 Other diseases of salivary glands
    • milk-alkali - E83.52 Hypercalcemia
    • Millard-Gubler - G46.3 Brain stem stroke syndrome
    • Miller-Dieker - Q93.88 Other microdeletions
    • Miller-Fisher - G61.0 Guillain-Barre syndrome
    • Minkowski-Chauffard - D58.0 Hereditary spherocytosis
    • Mirizzi's - K83.1 Obstruction of bile duct
    • MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy) - E88.49 Other mitochondrial metabolism disorders
    • Möbius, ophthalmoplegic migraine - See: Migraine, ophthalmoplegic;
    • monofixation - H50.42 Monofixation syndrome
    • Morel-Moore - M85.2 Hyperostosis of skull
    • Morel-Morgagni - M85.2 Hyperostosis of skull
    • Morgagni (-Morel) (-Stewart) - M85.2 Hyperostosis of skull
    • Morgagni-Adams-Stokes - I45.9 Conduction disorder, unspecified
    • Mounier-Kuhn - Q32.4 Other congenital malformations of bronchus
      • acquired - J98.09 Other diseases of bronchus, not elsewhere classified
        • with bronchiectasis - J47.9 Bronchiectasis, uncomplicated
          • with
            • exacerbation (acute) - J47.1 Bronchiectasis with (acute) exacerbation
            • lower respiratory infection - J47.0 Bronchiectasis with acute lower respiratory infection
      • with bronchiectasis - J47.9 Bronchiectasis, uncomplicated
        • with
          • exacerbation (acute) - J47.1 Bronchiectasis with (acute) exacerbation
          • lower respiratory infection - J47.0 Bronchiectasis with acute lower respiratory infection
    • Muckle-Wells - M04.2 Cryopyrin-associated periodic syndromes
    • mucocutaneous lymph node (acute febrile) (MCLS) - M30.3 Mucocutaneous lymph node syndrome [Kawasaki]
    • multiple endocrine neoplasia (MEN) - See: Neoplasia, endocrine, multiple (MEN);
    • multiple operations - See: Disorder, factitious;
    • multisystem inflammatory (in adults) (in children) - M35.81 Multisystem inflammatory syndrome
    • myasthenic - G70.9 Myoneural disorder, unspecified
      • in
        • diabetes mellitus - See: Diabetes, amyotrophy;
        • endocrine disease NEC - E34.9 Endocrine disorder, unspecified
        • neoplastic disease - See Also: Neoplasm; - D49.9 Neoplasm of unspecified behavior of unspecified site
        • thyrotoxicosis (hyperthyroidism) - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
          • with thyroid storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
    • myelodysplastic - D46.9 Myelodysplastic syndrome, unspecified
      • lesions, low grade - D46.20 Refractory anemia with excess of blasts, unspecified
      • specified NEC - D46.Z Other myelodysplastic syndromes
      • with
        • 5q deletion - D46.C Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality
        • isolated del (5q) chromosomal abnormality - D46.C Myelodysplastic syndrome with isolated del(5q) chromosomal abnormality
        • multilineage dysplasia - D46.A Refractory cytopenia with multilineage dysplasia
          • with ringed sideroblasts - D46.B Refractory cytopenia with multilineage dysplasia and ring sideroblasts
    • myeloid hypereosinophilic - D72.118 Other hypereosinophilic syndrome
    • myelopathic pain - G89.0 Central pain syndrome
    • myeloproliferative (chronic) - D47.1 Chronic myeloproliferative disease
    • myofascial pain - M79.18 Myalgia, other site
    • Naffziger's - G54.0 Brachial plexus disorders
    • nail patella - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • NARP (Neuropathy, Ataxia and Retinitis pigmentosa) - E88.49 Other mitochondrial metabolism disorders
    • neonatal abstinence - P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction
    • nephritic - See Also: Nephritis;
      • acute - N00.9 Acute nephritic syndrome with unspecified morphologic changes
      • chronic - N03.9 Chronic nephritic syndrome with unspecified morphologic changes
      • rapidly progressive - N01.9 Rapidly progressive nephritic syndrome with unspecified morphologic changes
      • with edema - See: Nephrosis;
    • nephrotic (congenital) - See Also: Nephrosis; - N04.9 Nephrotic syndrome with unspecified morphologic changes
      • diabetic - See: Diabetes, nephrosis;
      • with
        • C3
          • glomerulonephritis - N04.A Nephrotic syndrome with C3 glomerulonephritis
          • glomerulopathy - N04.A Nephrotic syndrome with C3 glomerulonephritis
            • with dense deposit disease - N04.6 Nephrotic syndrome with dense deposit disease
        • dense deposit disease - N04.6 Nephrotic syndrome with dense deposit disease
        • diffuse
          • crescentic glomerulonephritis - N04.7 Nephrotic syndrome with diffuse crescentic glomerulonephritis
          • endocapillary proliferative glomerulonephritis - N04.4 Nephrotic syndrome with diffuse endocapillary proliferative glomerulonephritis
          • membranous glomerulonephritis - N04.2 Nephrotic syndrome with diffuse membranous glomerulonephritis
          • mesangial proliferative glomerulonephritis - N04.3 Nephrotic syndrome with diffuse mesangial proliferative glomerulonephritis
          • mesangiocapillary glomerulonephritis - N04.5 Nephrotic syndrome with diffuse mesangiocapillary glomerulonephritis
        • focal and segmental glomerular lesions - N04.1 Nephrotic syndrome with focal and segmental glomerular lesions
        • minor glomerular abnormality - N04.0 Nephrotic syndrome with minor glomerular abnormality
        • specified morphological changes NEC - N04.8 Nephrotic syndrome with other morphologic changes
    • neurologic neglect - R41.4 Neurologic neglect syndrome
    • Nezelof's - D81.4 Nezelof's syndrome
    • Nonne-Milroy-Meige - Q82.0 Hereditary lymphedema
    • Nothnagel's vasomotor acroparesthesia - I73.89 Other specified peripheral vascular diseases
    • obesity hypoventilation (OHS) - E66.2 Morbid (severe) obesity with alveolar hypoventilation
    • oculomotor - H51.9 Unspecified disorder of binocular movement
    • Ogilvie - K59.81 Ogilvie syndrome
    • ophthalmoplegia-cerebellar ataxia - See: Strabismus, paralytic, third nerve;
    • oral allergy - T78.1 Other adverse food reactions, not elsewhere classified
    • oral-facial-digital - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • organic
      • affective - F06.30 Mood disorder due to known physiological condition, unspecified
      • amnesic (not alcohol- or drug-induced) - F04 Amnestic disorder due to known physiological condition
      • brain - F09 Unspecified mental disorder due to known physiological condition
      • depressive - F06.31 Mood disorder due to known physiological condition with depressive features
      • hallucinosis - F06.0 Psychotic disorder with hallucinations due to known physiological condition
      • personality - F07.0 Personality change due to known physiological condition
    • Ormond's - N13.5 Crossing vessel and stricture of ureter without hydronephrosis
    • oro-facial-digital - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • os trigonum - Q68.8 Other specified congenital musculoskeletal deformities
    • Osler-Weber-Rendu - I78.0 Hereditary hemorrhagic telangiectasia
    • osteoporosis-osteomalacia - M83.8 Other adult osteomalacia
    • Osterreicher-Turner - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • otolith
    • oto-palatal-digital - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • outlet (thoracic) - G54.0 Brachial plexus disorders
    • ovary
      • polycystic - E28.2 Polycystic ovarian syndrome
      • resistant - E28.39 Other primary ovarian failure
      • sclerocystic - E28.2 Polycystic ovarian syndrome
    • Owren's - D68.2 Hereditary deficiency of other clotting factors
    • Paget-Schroetter - I82.890 Acute embolism and thrombosis of other specified veins
    • pain - See Also: Pain;
      • complex regional I - G90.50 Complex regional pain syndrome I, unspecified
        • lower limb - G90.52 Complex regional pain syndrome I of lower limb
        • specified site NEC - G90.59 Complex regional pain syndrome I of other specified site
        • upper limb - G90.51 Complex regional pain syndrome I of upper limb
      • complex regional II - See: Causalgia;
    • painful
      • bruising - D69.2 Other nonthrombocytopenic purpura
      • feet - E53.8 Deficiency of other specified B group vitamins
      • prostate - N42.81 Prostatodynia syndrome
    • paralysis agitans - See: Parkinsonism;
    • paralytic - G83.9 Paralytic syndrome, unspecified
      • specified NEC - G83.89 Other specified paralytic syndromes
    • Parinaud's - H51.0 Palsy (spasm) of conjugate gaze
    • parkinsonian - See: Parkinsonism;
    • Parkinson's - See: Parkinsonism;
    • paroxysmal facial pain - G50.0 Trigeminal neuralgia
    • Parry's - E05.00 Thyrotoxicosis with diffuse goiter without thyrotoxic crisis or storm
      • with thyroid storm - E05.01 Thyrotoxicosis with diffuse goiter with thyrotoxic crisis or storm
    • Parsonage (-Aldren)-Turner - G54.5 Neuralgic amyotrophy
    • patella clunk - M25.86 Other specified joint disorders, knee
    • Paterson (-Brown) (-Kelly) - D50.1 Sideropenic dysphagia
    • pectoral girdle - I77.89 Other specified disorders of arteries and arterioles
    • pectoralis minor - I77.89 Other specified disorders of arteries and arterioles
    • pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections (PANDAS) - D89.89 Other specified disorders involving the immune mechanism, not elsewhere classified
    • pediatric inflammatory multisystem - M35.81 Multisystem inflammatory syndrome
    • Pelger-Huet - D72.0 Genetic anomalies of leukocytes
    • pellagra-cerebellar ataxia-renal aminoaciduria - E72.02 Hartnup's disease
    • pellagroid - E52 Niacin deficiency [pellagra]
    • Pellegrini-Stieda - See: Bursitis, tibial collateral;
    • pelvic congestion-fibrosis, female - N94.89 Other specified conditions associated with female genital organs and menstrual cycle
    • penta X - Q97.1 Female with more than three X chromosomes
    • peptic ulcer - See: Ulcer, peptic;
    • perabduction - I77.89 Other specified disorders of arteries and arterioles
    • periodic fever - M04.1 Periodic fever syndromes
    • periodic fever, aphthous stomatitis, pharyngitis, and adenopathy [PFAPA] - M04.8 Other autoinflammatory syndromes
    • periodic headache, in adults and children - See: Headache, periodic syndromes in adults and children;
    • periurethral fibrosis - N13.5 Crossing vessel and stricture of ureter without hydronephrosis
    • Peutz-Jeghers - Q85.89 Other phakomatoses, not elsewhere classified
    • phantom limb (without pain) - G54.7 Phantom limb syndrome without pain
      • with pain - G54.6 Phantom limb syndrome with pain
    • pharyngeal pouch - D82.1 Di George's syndrome
    • Pick's - See: Disease, Pick's;
    • Pickwickian - E66.2 Morbid (severe) obesity with alveolar hypoventilation
    • PIE (pulmonary infiltration with eosinophilia) - See Also: Eosinophilia, pulmonary; - J82.89 Other pulmonary eosinophilia, not elsewhere classified
    • pigmentary pallidal degeneration (progressive) - G23.0 Hallervorden-Spatz disease
    • pineal - E34.8 Other specified endocrine disorders
    • pituitary - E22.0 Acromegaly and pituitary gigantism
    • placental transfusion - See: Pregnancy, complicated by, placental transfusion syndromes;
    • plantar fascia - M72.2 Plantar fascial fibromatosis
    • plateau iris (post-iridectomy) (postprocedural) - H21.82 Plateau iris syndrome (post-iridectomy) (postprocedural)
    • Plummer-Vinson - D50.1 Sideropenic dysphagia
    • pluricarential of infancy - E40 Kwashiorkor
    • plurideficiency - E40 Kwashiorkor
    • pluriglandular (compensatory) - E31.8 Other polyglandular dysfunction
      • autoimmune - E31.0 Autoimmune polyglandular failure
    • pneumatic hammer - T75.21 Pneumatic hammer syndrome
    • polyangiitis overlap - M30.8 Other conditions related to polyarteritis nodosa
    • polycarential of infancy - E40 Kwashiorkor
    • polyglandular - E31.8 Other polyglandular dysfunction
      • autoimmune - E31.0 Autoimmune polyglandular failure
    • polysplenia - Q89.09 Congenital malformations of spleen
    • pontine NEC - G93.89 Other specified disorders of brain
    • popliteal
      • artery entrapment - I77.89 Other specified disorders of arteries and arterioles
      • web - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • post chemoembolization - code to associated conditions
    • post endometrial ablation - N99.85 Post endometrial ablation syndrome
    • postbacterial fatigue - G93.39 Other post infection and related fatigue syndromes
    • postcardiac injury
      • postcardiotomy - I97.0 Postcardiotomy syndrome
      • postmyocardial infarction - I24.1 Dressler's syndrome
    • postcardiotomy - I97.0 Postcardiotomy syndrome
    • postcholecystectomy - K91.5 Postcholecystectomy syndrome
    • postcommissurotomy - I97.0 Postcardiotomy syndrome
    • postconcussional - F07.81 Postconcussional syndrome
    • postcontusional - F07.81 Postconcussional syndrome
    • post-COVID (-19) - U09.9 Post COVID-19 condition, unspecified
    • postencephalitic - F07.89 Other personality and behavioral disorders due to known physiological condition
    • posterior
      • cervical sympathetic - M53.0 Cervicocranial syndrome
      • cord - G83.83 Posterior cord syndrome
      • fossa compression - G93.5 Compression of brain
      • reversible encephalopathy (PRES) - I67.83 Posterior reversible encephalopathy syndrome
    • postgastrectomy (dumping) - K91.1 Postgastric surgery syndromes
    • postgastric surgery - K91.1 Postgastric surgery syndromes
    • postinfarction - I24.1 Dressler's syndrome
    • postinfectious fatigue - G93.39 Other post infection and related fatigue syndromes
    • postlaminectomy NEC - M96.1 Postlaminectomy syndrome, not elsewhere classified
    • postleukotomy - F07.0 Personality change due to known physiological condition
    • postmastectomy lymphedema - I97.2 Postmastectomy lymphedema syndrome
    • postmyocardial infarction - I24.1 Dressler's syndrome
    • postoperative NEC - T81.9 Unspecified complication of procedure
      • blind loop - K90.2 Blind loop syndrome, not elsewhere classified
    • postpartum panhypopituitary (Sheehan) - E23.0 Hypopituitarism
    • postpolio (myelitic) - G14 Postpolio syndrome
    • postthrombotic - I87.009 Postthrombotic syndrome without complications of unspecified extremity
      • asymptomatic - I87.00 Postthrombotic syndrome without complications
      • with
        • inflammation - I87.02 Postthrombotic syndrome with inflammation
          • with ulcer - I87.03 Postthrombotic syndrome with ulcer and inflammation
        • specified complication NEC - I87.09 Postthrombotic syndrome with other complications
        • ulcer - I87.01 Postthrombotic syndrome with ulcer
          • with inflammation - I87.03 Postthrombotic syndrome with ulcer and inflammation
    • postural
      • orthostatic tachycardia [POTS] - G90.A Postural orthostatic tachycardia syndrome [POTS]
      • tachycardia - G90.A Postural orthostatic tachycardia syndrome [POTS]
    • postvagotomy - K91.1 Postgastric surgery syndromes
    • postvalvulotomy - I97.0 Postcardiotomy syndrome
    • postviral NEC - G93.31 Postviral fatigue syndrome
      • fatigue - G93.31 Postviral fatigue syndrome
    • Potain's - K31.0 Acute dilatation of stomach
    • potassium intoxication - E87.5 Hyperkalemia
    • Prader-Willi - Q87.11 Prader-Willi syndrome
    • Prader-Willi-like - Q87.19 Other congenital malformation syndromes predominantly associated with short stature
    • precerebral artery (multiple) (bilateral) - G45.2 Multiple and bilateral precerebral artery syndromes
    • preinfarction - I20.0 Unstable angina
    • preleukemic - D46.9 Myelodysplastic syndrome, unspecified
    • premature senility - E34.8 Other specified endocrine disorders
    • premenstrual dysphoric - F32.81 Premenstrual dysphoric disorder
    • premenstrual tension - N94.3 Premenstrual tension syndrome
    • Prinzmetal-Massumi - R07.1 Chest pain on breathing
    • prune belly - Q79.4 Prune belly syndrome
    • pseudo -Turner's - Q87.19 Other congenital malformation syndromes predominantly associated with short stature
    • pseudocarpal tunnel (sublimis) - See: Syndrome, carpal tunnel;
    • pseudoparalytica - G70.00 Myasthenia gravis without (acute) exacerbation
      • in crisis - G70.01 Myasthenia gravis with (acute) exacerbation
      • with exacerbation (acute) - G70.01 Myasthenia gravis with (acute) exacerbation
    • psycho-organic (nonpsychotic severity) - F07.9 Unspecified personality and behavioral disorder due to known physiological condition
      • acute or subacute - F05 Delirium due to known physiological condition
      • depressive type - F06.31 Mood disorder due to known physiological condition with depressive features
      • hallucinatory type - F06.0 Psychotic disorder with hallucinations due to known physiological condition
      • nonpsychotic severity - F07.0 Personality change due to known physiological condition
      • specified NEC - F07.89 Other personality and behavioral disorders due to known physiological condition
    • PTEN (hamartoma) tumor - Q85.81 PTEN tumor syndrome
    • pulmonary
      • arteriosclerosis - I27.0 Primary pulmonary hypertension
      • dysmaturity (Wilson-Mikity) - P27.0 Wilson-Mikity syndrome
      • hypoperfusion (idiopathic) - P22.0 Respiratory distress syndrome of newborn
      • renal (hemorrhagic) (Goodpasture's) - M31.0 Hypersensitivity angiitis
    • pure
      • motor lacunar - G46.5 Pure motor lacunar syndrome
      • sensory lacunar - G46.6 Pure sensory lacunar syndrome
    • Putnam-Dana - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
    • pyogenic arthritis, pyoderma gangrenosum, and acne [PAPA] - M04.8 Other autoinflammatory syndromes
    • pyramidopallidonigral - G20 Parkinson's disease
    • pyriformis - See: Lesion, nerve, sciatic;
    • QT interval prolongation - I45.81 Long QT syndrome
    • radicular NEC - See: Radiculopathy;
      • upper limbs, newborn (birth injury) - P14.3 Other brachial plexus birth injuries
    • rapid time-zone change - G47.25 Circadian rhythm sleep disorder, jet lag type
    • Rasmussen - G04.81 Other encephalitis and encephalomyelitis
    • Raymond (-Céstan) - I65.8 Occlusion and stenosis of other precerebral arteries
    • Raynaud's - I73.00 Raynaud's syndrome without gangrene
      • with gangrene - I73.01 Raynaud's syndrome with gangrene
    • RDS (respiratory distress syndrome, newborn) - P22.0 Respiratory distress syndrome of newborn
    • reactive airways dysfunction - J68.3 Other acute and subacute respiratory conditions due to chemicals, gases, fumes and vapors
    • Refsum's - G60.1 Refsum's disease
    • Reifenstein - E34.52 Partial androgen insensitivity syndrome
    • renal glomerulohyalinosis-diabetic - See: Diabetes, nephrosis;
    • Rendu-Osler-Weber - I78.0 Hereditary hemorrhagic telangiectasia
    • residual ovary - N99.83 Residual ovary syndrome
    • resistant ovary - E28.39 Other primary ovarian failure
    • respiratory
      • distress
        • acute - J80 Acute respiratory distress syndrome
          • adult - J80 Acute respiratory distress syndrome
          • child - J80 Acute respiratory distress syndrome
          • idiopathic - J84.114 Acute interstitial pneumonitis
        • newborn (idiopathic) (type I) - P22.0 Respiratory distress syndrome of newborn
          • type II - P22.1 Transient tachypnea of newborn
    • restless legs - G25.81 Restless legs syndrome
    • retinoblastoma (familial) - C69.2 Malignant neoplasm of retina
    • retroperitoneal fibrosis - N13.5 Crossing vessel and stricture of ureter without hydronephrosis
    • retroviral seroconversion (acute) - Z21 Asymptomatic human immunodeficiency virus [HIV] infection status
    • Reye's - G93.7 Reye's syndrome
    • Richter - See: Leukemia, chronic lymphocytic, B-cell type;
    • Ridley's - I50.1 Left ventricular failure, unspecified
    • right
      • heart, hypoplastic - Q22.6 Hypoplastic right heart syndrome
      • ventricular obstruction - See: Failure, heart, right;
    • Romano-Ward (prolonged QT interval) - I45.81 Long QT syndrome
    • rotator cuff, shoulder - See Also: Tear, rotator cuff; - M75.10 Unspecified rotator cuff tear or rupture, not specified as traumatic
    • Rotes Quérol - See: Hyperostosis, ankylosing;
    • Roth - See: Meralgia paresthetica;
    • rubella (congenital) - P35.0 Congenital rubella syndrome
    • Ruvalcaba-Myhre-Smith - E71.440 Ruvalcaba-Myhre-Smith syndrome
    • Rytand-Lipsitch - I44.2 Atrioventricular block, complete
    • salt
      • depletion - E87.1 Hypo-osmolality and hyponatremia
        • due to heat NEC - T67.8 Other effects of heat and light
          • causing heat exhaustion or prostration - T67.4 Heat exhaustion due to salt depletion
      • low - E87.1 Hypo-osmolality and hyponatremia
    • salt-losing - N28.89 Other specified disorders of kidney and ureter
    • SATB2-associated - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
    • Scaglietti-Dagnini - E22.0 Acromegaly and pituitary gigantism
    • scalenus anticus (anterior) - G54.0 Brachial plexus disorders
    • scapulocostal - See: Mononeuropathy, upper limb, specified site NEC;
    • scapuloperoneal - G71.09 Other specified muscular dystrophies
    • schizophrenic, of childhood NEC - F84.5 Asperger's syndrome
    • Schnitzler - D47.2 Monoclonal gammopathy
    • Scholte's - E34.0 Carcinoid syndrome
    • Schroeder's - E27.0 Other adrenocortical overactivity
    • Schüller-Christian - C96.5 Multifocal and unisystemic Langerhans-cell histiocytosis
    • Schwachman's - See: Syndrome, Shwachman's;
    • Schwartz (-Jampel) - G71.13 Myotonic chondrodystrophy
    • Schwartz-Bartter - E22.2 Syndrome of inappropriate secretion of antidiuretic hormone
    • scimitar - Q26.8 Other congenital malformations of great veins
    • sclerocystic ovary - E28.2 Polycystic ovarian syndrome
    • Seitelberger's - G31.89 Other specified degenerative diseases of nervous system
    • septicemic adrenal hemorrhage - A39.1 Waterhouse-Friderichsen syndrome
    • seroconversion, retroviral (acute) - Z21 Asymptomatic human immunodeficiency virus [HIV] infection status
    • serous meningitis - G93.2 Benign intracranial hypertension
    • severe acute respiratory (SARS) - J12.81 Pneumonia due to SARS-associated coronavirus
      • coronavirus 2 - See Also: COVID-19; - U07.1 COVID-19
        • pneumonia - J12.82 Pneumonia due to coronavirus disease 2019
    • shaken infant - T74.4 Shaken infant syndrome
    • shock (traumatic) - T79.4 Traumatic shock
      • kidney - N17.0 Acute kidney failure with tubular necrosis
        • following crush injury - T79.5 Traumatic anuria
      • toxic - A48.3 Toxic shock syndrome
    • shock-lung - J80 Acute respiratory distress syndrome
    • Shone's - code to specific anomalies
    • short
      • bowel - K91.2 Postsurgical malabsorption, not elsewhere classified
      • rib - Q77.2 Short rib syndrome
    • shoulder-hand - See: Algoneurodystrophy;
    • Shwachman's - D70.4 Cyclic neutropenia
    • sicca - See: Syndrome, Sjögren;
    • sick
      • cell - E87.1 Hypo-osmolality and hyponatremia
      • sinus - I49.5 Sick sinus syndrome
    • sick-euthyroid - E07.81 Sick-euthyroid syndrome
    • sideropenic - D50.1 Sideropenic dysphagia
    • Siemens' ectodermal dysplasia - Q82.4 Ectodermal dysplasia (anhidrotic)
    • Silfversköld's - Q78.9 Osteochondrodysplasia, unspecified
    • Simons' - E88.1 Lipodystrophy, not elsewhere classified
    • sinus tarsi - M25.57 Pain in ankle and joints of foot
    • sinusitis-bronchiectasis-situs inversus - Q89.3 Situs inversus
    • Sipple's - E31.22 Multiple endocrine neoplasia [MEN] type IIA
    • sirenomelia - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • Sjögren - M35.00 Sjogren syndrome, unspecified
      • with
        • central nervous system involvement - M35.07 Sjogren syndrome with central nervous system involvement
        • dental involvement - M35.0C Sjogren syndrome with dental involvement
        • gastrointestinal involvement - M35.08 Sjogren syndrome with gastrointestinal involvement
        • glomerular disease - M35.0A Sjogren syndrome with glomerular disease
        • inflammatory arthritis - M35.05 Sjogren syndrome with inflammatory arthritis
        • keratoconjunctivitis - M35.01 Sjogren syndrome with keratoconjunctivitis
        • lung involvement - M35.02 Sjogren syndrome with lung involvement
        • myopathy - M35.03 Sjogren syndrome with myopathy
        • peripheral nervous system involvement - M35.06 Sjogren syndrome with peripheral nervous system involvement
        • renal tubular acidosis - M35.04 Sjogren syndrome with tubulo-interstitial nephropathy
        • specified organ involvement, NEC - M35.09 Sjogren syndrome with other organ involvement
        • tubulo-interstitial nephropathy - M35.04 Sjogren syndrome with tubulo-interstitial nephropathy
        • vasculitis - M35.0B Sjogren syndrome with vasculitis
    • Slocumb's - E27.0 Other adrenocortical overactivity
    • slow flow, coronary - I20.8 Other forms of angina pectoris
    • Sluder's - G44.89 Other headache syndrome
    • Smith-Magenis - Q93.88 Other microdeletions
    • Sneddon-Wilkinson - L13.1 Subcorneal pustular dermatitis
    • Soto's - Q87.3 Congenital malformation syndromes involving early overgrowth
    • South African cardiomyopathy - I42.8 Other cardiomyopathies
    • spasmodic
      • upward movement, eyes - H51.8 Other specified disorders of binocular movement
      • winking - F95.8 Other tic disorders
    • Spen's - I45.9 Conduction disorder, unspecified
    • splenic
      • agenesis - Q89.01 Asplenia (congenital)
      • flexure - K59.89 Other specified functional intestinal disorders
      • neutropenia - D73.81 Neutropenic splenomegaly
    • Spurway's - Q78.0 Osteogenesis imperfecta
    • staphylococcal scalded skin - L00 Staphylococcal scalded skin syndrome
    • steal
      • arteriovenous - T82.898 Other specified complication of vascular prosthetic devices, implants and grafts
      • ischemic - T82.898 Other specified complication of vascular prosthetic devices, implants and grafts
      • subclavian - G45.8 Other transient cerebral ischemic attacks and related syndromes
    • Stein-Leventhal - E28.2 Polycystic ovarian syndrome
    • Stein's - E28.2 Polycystic ovarian syndrome
    • Stevens-Johnson syndrome - L51.1 Stevens-Johnson syndrome
      • toxic epidermal necrolysis overlap - L51.3 Stevens-Johnson syndrome-toxic epidermal necrolysis overlap syndrome
    • Stewart-Morel - M85.2 Hyperostosis of skull
    • Stickler - Q89.8 Other specified congenital malformations
    • stiff baby - Q89.8 Other specified congenital malformations
    • stiff man - G25.82 Stiff-man syndrome
    • Still-Felty - See: Felty's syndrome;
    • Stokes (-Adams) - I45.9 Conduction disorder, unspecified
    • stone heart - I50.1 Left ventricular failure, unspecified
    • straight back, congenital - Q76.49 Other congenital malformations of spine, not associated with scoliosis
    • Sturge-Weber (-Dimitri) - Q85.89 Other phakomatoses, not elsewhere classified
    • subclavian steal - G45.8 Other transient cerebral ischemic attacks and related syndromes
    • subcoracoid-pectoralis minor - G54.0 Brachial plexus disorders
    • subcostal nerve compression - I77.89 Other specified disorders of arteries and arterioles
    • subphrenic interposition - Q43.3 Congenital malformations of intestinal fixation
    • superior
      • cerebellar artery - I63.89 Other cerebral infarction
      • mesenteric artery - K55.1 Chronic vascular disorders of intestine
      • semi-circular canal dehiscence - H83.8X Other specified diseases of inner ear
      • vena cava - I87.1 Compression of vein
    • supine hypotensive (maternal) - See: Syndrome, hypotension, maternal;
    • suprarenal cortical - E27.0 Other adrenocortical overactivity
    • supraspinatus - See Also: Tear, rotator cuff; - M75.10 Unspecified rotator cuff tear or rupture, not specified as traumatic
    • Susac - G93.49 Other encephalopathy
    • swallowed blood - P78.2 Neonatal hematemesis and melena due to swallowed maternal blood
    • sweat retention - L74.0 Miliaria rubra
    • Swyer - Q99.1 46, XX true hermaphrodite
    • Symond's - G93.2 Benign intracranial hypertension
    • sympathetic
      • cervical paralysis - G90.2 Horner's syndrome
      • pelvic, female - N94.89 Other specified conditions associated with female genital organs and menstrual cycle
    • systemic inflammatory response (SIRS), of non-infectious origin (without organ dysfunction) - R65.10 Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ dysfunction
      • with acute organ dysfunction - R65.11 Systemic inflammatory response syndrome (SIRS) of non-infectious origin with acute organ dysfunction
    • tachycardia-bradycardia - I49.5 Sick sinus syndrome
    • takotsubo - I51.81 Takotsubo syndrome
    • TAR (thrombocytopenia with absent radius) - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • tarsal tunnel - G57.5 Tarsal tunnel syndrome
    • teething - K00.7 Teething syndrome
    • tegmental - G93.89 Other specified disorders of brain
    • telangiectasic-pigmentation-cataract - Q82.8 Other specified congenital malformations of skin
    • temporal pyramidal apex - See: Otitis, media, suppurative, acute;
    • temporomandibular joint-pain-dysfunction - M26.62 Arthralgia of temporomandibular joint
    • Terry's - See Also: Myopia, degenerative; - H44.2 Degenerative myopia
    • testicular feminization - See Also: Syndrome, androgen insensitivity; - E34.51 Complete androgen insensitivity syndrome
    • thalamic pain (hyperesthetic) - G89.0 Central pain syndrome
    • thoracic outlet (compression) - G54.0 Brachial plexus disorders
    • Thorson-Björck - E34.0 Carcinoid syndrome
    • thrombocytopenia with absent radius (TAR) - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • thrombosis with thrombocytopenia - D75.84 Other platelet-activating anti-PF4 disorders
    • thyroid-adrenocortical insufficiency - E31.0 Autoimmune polyglandular failure
    • tibial
      • anterior - M76.81 Anterior tibial syndrome
      • posterior - M76.82 Posterior tibial tendinitis
    • Tietze's - M94.0 Chondrocostal junction syndrome [Tietze]
    • time-zone (rapid) - G47.25 Circadian rhythm sleep disorder, jet lag type
    • Toni-Fanconi - E72.09 Other disorders of amino-acid transport
      • with cystinosis - E72.04 Cystinosis
    • Touraine's - Q79.8 Other congenital malformations of musculoskeletal system
    • tourniquet - See: Constriction, external, by site;
    • toxic shock - A48.3 Toxic shock syndrome
    • transient left ventricular apical ballooning - I51.81 Takotsubo syndrome
    • traumatic vasospastic - T75.22 Traumatic vasospastic syndrome
    • Treacher Collins - Q75.4 Mandibulofacial dysostosis
    • triple X, female - Q97.0 Karyotype 47, XXX
    • trisomy - Q92.9 Trisomy and partial trisomy of autosomes, unspecified
      • 13 - Q91.7 Trisomy 13, unspecified
        • meiotic nondisjunction - Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction)
        • mitotic nondisjunction - Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)
        • mosaicism - Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)
        • translocation - Q91.6 Trisomy 13, translocation
      • 18 - Q91.3 Trisomy 18, unspecified
        • meiotic nondisjunction - Q91.0 Trisomy 18, nonmosaicism (meiotic nondisjunction)
        • mitotic nondisjunction - Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)
        • mosaicism - Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)
        • translocation - Q91.2 Trisomy 18, translocation
      • 20 (q) (p) - Q92.8 Other specified trisomies and partial trisomies of autosomes
      • 21 - Q90.9 Down syndrome, unspecified
        • meiotic nondisjunction - Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction)
        • mitotic nondisjunction - Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
        • mosaicism - Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
        • translocation - Q90.2 Trisomy 21, translocation
      • 22 - Q92.8 Other specified trisomies and partial trisomies of autosomes
    • tropical wet feet - T69.0 Immersion hand and foot
    • Trousseau's - I82.1 Thrombophlebitis migrans
    • tumor lysis (following antineoplastic chemotherapy) (spontaneous) NEC - E88.3 Tumor lysis syndrome
    • tumor necrosis factor receptor associated periodic (TRAPS) - M04.1 Periodic fever syndromes
    • Twiddler's (due to)
      • automatic implantable defibrillator - T82.198 Other mechanical complication of other cardiac electronic device
      • cardiac pacemaker - T82.198 Other mechanical complication of other cardiac electronic device
    • Unverricht (-Lundborg) - See: Epilepsy, generalized, idiopathic;
    • upward gaze - H51.8 Other specified disorders of binocular movement
    • uremia, chronic - See Also: Disease, kidney, chronic; - N18.9 Chronic kidney disease, unspecified
    • urethral - N34.3 Urethral syndrome, unspecified
    • urethro-oculo-articular - See: Reiter's disease;
    • urohepatic - K76.7 Hepatorenal syndrome
    • vago-hypoglossal - G52.7 Disorders of multiple cranial nerves
    • van Buchem's - M85.2 Hyperostosis of skull
    • van der Hoeve's - Q78.0 Osteogenesis imperfecta
    • vascular NEC in cerebrovascular disease - G46.8 Other vascular syndromes of brain in cerebrovascular diseases
    • vasoconstriction, reversible cerebrovascular - I67.841 Reversible cerebrovascular vasoconstriction syndrome
    • vasomotor - I73.9 Peripheral vascular disease, unspecified
    • vasospastic (traumatic) - T75.22 Traumatic vasospastic syndrome
    • vasovagal - R55 Syncope and collapse
    • VATER - Q87.2 Congenital malformation syndromes predominantly involving limbs
    • velo-cardio-facial - Q93.81 Velo-cardio-facial syndrome
    • vena cava (inferior) (superior) (obstruction) - I87.1 Compression of vein
    • vertebral
      • artery - G45.0 Vertebro-basilar artery syndrome
        • compression - See: Syndrome, anterior, spinal artery, compression;
      • steal - G45.0 Vertebro-basilar artery syndrome
    • vertebro-basilar artery - G45.0 Vertebro-basilar artery syndrome
    • vertebrogenic (pain) - See Also: Pain, vertebrogenic; - M54.89 Other dorsalgia
    • vertiginous - See: Disorder, vestibular function;
    • Vinson-Plummer - D50.1 Sideropenic dysphagia
    • virus - B34.9 Viral infection, unspecified
    • visceral larva migrans - B83.0 Visceral larva migrans
    • visual disorientation - H53.8 Other visual disturbances
    • vitamin B6 deficiency - E53.1 Pyridoxine deficiency
    • vitreal corneal - H59.01 Keratopathy (bullous aphakic) following cataract surgery
    • vitreous (touch) - H59.01 Keratopathy (bullous aphakic) following cataract surgery
    • Vogt-Koyanagi - H20.82 Vogt-Koyanagi syndrome
    • Volkmann's - T79.6 Traumatic ischemia of muscle
    • von Hippel-Lindau - Q85.83 Von Hippel-Lindau syndrome
    • von Schroetter's - I82.890 Acute embolism and thrombosis of other specified veins
    • von Willebrand (-Jürgen) - See: Disease, von Willebrand;
      • acquired - See Also: Disease, von Willebrand; - D68.04 Acquired von Willebrand disease
    • Waldenström-Kjellberg - D50.1 Sideropenic dysphagia
    • Wallenberg's - G46.3 Brain stem stroke syndrome
    • water retention - E87.79 Other fluid overload
    • Waterhouse (-Friderichsen) - A39.1 Waterhouse-Friderichsen syndrome
    • Weber-Gubler - G46.3 Brain stem stroke syndrome
    • Weber-Leyden - G46.3 Brain stem stroke syndrome
    • Weber's - G46.3 Brain stem stroke syndrome
    • Wegener's - M31.30 Wegener's granulomatosis without renal involvement
      • with
        • kidney involvement - M31.31 Wegener's granulomatosis with renal involvement
        • lung involvement - M31.30 Wegener's granulomatosis without renal involvement
          • with kidney involvement - M31.31 Wegener's granulomatosis with renal involvement
    • Weingarten's (tropical eosinophilia) - J82.89 Other pulmonary eosinophilia, not elsewhere classified
    • Weiss-Baker - G90.09 Other idiopathic peripheral autonomic neuropathy
    • Werdnig-Hoffman - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
    • Wermer's - E31.21 Multiple endocrine neoplasia [MEN] type I
    • Werner's - E34.8 Other specified endocrine disorders
    • Wernicke-Korsakoff (nonalcoholic) - F04 Amnestic disorder due to known physiological condition
      • alcoholic - F10.26 Alcohol dependence with alcohol-induced persisting amnestic disorder
    • Westphal-Strümpell - E83.01 Wilson's disease
    • West's - See: Epilepsy, spasms;
    • wet
      • feet (maceration) (tropical) - T69.0 Immersion hand and foot
      • lung, newborn - P22.1 Transient tachypnea of newborn
    • whiplash - S13.4 Sprain of ligaments of cervical spine
    • whistling face - Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
    • Wilkie's - K55.1 Chronic vascular disorders of intestine
    • Wilkinson-Sneddon - L13.1 Subcorneal pustular dermatitis
    • Willebrand (-Jürgens) - See: Disease, von Willebrand;
    • Williams - Q93.82 Williams syndrome
    • Wilson's (hepatolenticular degeneration) - E83.01 Wilson's disease
    • Wiskott-Aldrich - D82.0 Wiskott-Aldrich syndrome
    • withdrawal - See: Withdrawal, state;
      • drug
        • infant of dependent mother - P96.1 Neonatal withdrawal symptoms from maternal use of drugs of addiction
        • therapeutic use, newborn - P96.2 Withdrawal symptoms from therapeutic use of drugs in newborn
    • Woakes' (ethmoiditis) - J33.1 Polypoid sinus degeneration
    • Wright's (hyperabduction) - G54.0 Brachial plexus disorders
    • X - I20.9 Angina pectoris, unspecified
    • XXXX - Q97.1 Female with more than three X chromosomes
    • XXXXX - Q97.1 Female with more than three X chromosomes
    • XXXXY - Q98.1 Klinefelter syndrome, male with more than two X chromosomes
    • XXY - Q98.0 Klinefelter syndrome karyotype 47, XXY
    • Yao - M04.8 Other autoinflammatory syndromes
    • yellow nail - L60.5 Yellow nail syndrome
    • Zahorsky's - B08.5 Enteroviral vesicular pharyngitis
    • Zellweger syndrome - E71.510 Zellweger syndrome
    • Zellweger-like syndrome - E71.541 Zellweger-like syndrome