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
- abnormal innervation - H02.519 Abnormal innervation syndrome unspecified eye, unspecified 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
- 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
- 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
- compression - M47.019 Anterior spinal artery compression syndromes, site unspecified
- tibial - M76.81 Anterior tibial syndrome
- antibody deficiency - D80.9 Immunodeficiency with predominantly antibody defects, unspecified
- anticardiolipin (-antibody) - D68.61 Antiphospholipid syndrome
- antidepressant discontinuation - T43.205 Adverse effect of unspecified antidepressants
- antiphospholipid (-antibody) - D68.61 Antiphospholipid syndrome
- aortic
- 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
- 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
- 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
- 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
- central pain - G89.0 Central pain syndrome
- cerebellar
- cerebellomedullary malformation - See: Spina bifida;
- cerebral
- cervical (root) - M53.1 Cervicobrachial 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
- 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
- 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
- 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
- coronary
- 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
- 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
- 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;
- 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
- 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
- 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
- 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;
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- hemolytic-uremic - D59.30 Hemolytic-uremic syndrome, unspecified
- atypical - 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
- 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
- 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
- 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)
- 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
- 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
- grade
- 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
- 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
- intravascular coagulation-fibrinolysis (ICF) - D65 Disseminated intravascular coagulation [defibrination syndrome]
- iodine-deficiency, congenital - E00.9 Congenital iodine-deficiency syndrome, unspecified
- IRDS (idiopathic respiratory distress, newborn) - P22.0 Respiratory distress syndrome of newborn
- irritable
- ischemic
- 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
- Landau-Kleffner - See: Epilepsy, specified NEC;
- Larsen's - Q74.8 Other specified congenital malformations of limb(s)
- lateral
- Launois' - E22.0 Acromegaly and pituitary gigantism
- lazy
- Lemiere - I80.8 Phlebitis and thrombophlebitis of other sites
- Lennox-Gastaut - 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
- 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
- malignant
- 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
- cardiovascular manifestations - Q87.418 Marfan's syndrome with other cardiovascular manifestations
- with
- 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
- 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
- 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
- in
- 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;
- nephrotic (congenital) - See Also: Nephrosis; - N04.9 Nephrotic syndrome with unspecified morphologic changes
- diabetic - See: Diabetes, nephrosis;
- with
- C3
- 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
- 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
- complex regional II - See: Causalgia;
- painful
- 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
- 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
- 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
- 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
- inflammation - I87.02 Postthrombotic syndrome with inflammation
- postural
- postvagotomy - K91.1 Postgastric surgery syndromes
- postvalvulotomy - I97.0 Postcardiotomy 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
- 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
- pure
- 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
- 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
- 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
- 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
- serous meningitis - G93.2 Benign intracranial hypertension
- severe acute respiratory (SARS) - J12.81 Pneumonia due to SARS-associated coronavirus
- shaken infant - T74.4 Shaken infant syndrome
- shock (traumatic) - T79.4 Traumatic shock
- shock-lung - J80 Acute respiratory distress syndrome
- Shone's - code to specific anomalies
- short
- shoulder-hand - See: Algoneurodystrophy;
- Shwachman's - D70.4 Cyclic neutropenia
- sicca - See: Syndrome, Sjögren;
- sick
- 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
- with
- 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
- Spen's - I45.9 Conduction disorder, unspecified
- splenic
- Spurway's - Q78.0 Osteogenesis imperfecta
- staphylococcal scalded skin - L00 Staphylococcal scalded skin syndrome
- steal
- 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
- 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
- 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
- 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
- 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)
- 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
- 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
- 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
- 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;
- 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