ICD-10-CM Syndrome References
"Syndrome" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries
Browse the ICD-10-CM codes with references applicable to the clinical term "syndrome"
- Syndrome - See Also: Disease;
- 22q13.3 deletion - Q93.52 Phelan-McDermid syndrome
- 48,XXXX - Q97.1 Female with more than three X chromosomes
- 49,XXXXX - Q97.1 Female with more than three X chromosomes
- 4H - G11.5 Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- 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
- Aicardi-Goutières - E79.81 Aicardi-Goutieres syndrome
- Alagille (-Watson) - Q44.71 Alagille syndrome
- 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 - E34.09 Other 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
- Axenfeld-Rieger - Q13.81 Rieger anomaly
- Ayerza (-Arrillaga) - I27.0 Primary pulmonary hypertension
- Babinski-Nageotte - G83.89 Other specified paralytic syndromes
- Bakwin-Krida - Q78.5 Metaphyseal dysplasia
- Bardet-Biedl - Q87.83 Bardet-Biedl syndrome
- 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 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) - E34.09 Other 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
- bronchiolitis obliterans - See Also: Bronchiolitis, obliterative; - J44.81 Bronchiolitis obliterans and bronchiolitis obliterans syndrome
- 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 - E34.00 Carcinoid syndrome, unspecified
- 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) - E34.09 Other 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 - See Also: Syndrome, thoracic 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 - E88.810 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
- 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 - E34.09 Other 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 - G90.89 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 - I20.89 Other forms of angina pectoris
- Hedinger's - E34.01 Carcinoid heart 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
- Hunt's (herpetic geniculate ganglionitis) (neuralgia) - B02.21 Postherpetic geniculate ganglionitis
- dyssynergia cerebellaris myoclonica - G11.19 Other early-onset cerebellar ataxia
- 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 (see also, Diabetes, by type, with 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
- insulin resistance
- 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
- Kimmelstiel-Wilson - See: Diabetes, specified type, with Kimmelstiel-Wilson disease;
- Kleefstra - Q87.86 Kleefstra syndrome
- Klein (e)-Levine - G47.13 Recurrent hypersomnia
- Klippel-Feil (brevicollis) - Q76.1 Klippel-Feil syndrome
- Köhler-Pellegrini-Stieda - 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)
- Lassueur Graham-Little Piccardi - L66.19 Other lichen planopilaris
- lateral
- Launois' - E22.0 Acromegaly and pituitary gigantism
- Laurence-Moon - Q87.84 Laurence-Moon syndrome
- lazy
- Lemierre - 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 - I20.89 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 - Q87.40 Marfan syndrome, unspecified
- with
- cardiovascular manifestations - Q87.418 Marfan syndrome with other cardiovascular manifestations
- aortic dilation - Q87.410 Marfan syndrome with aortic dilation
- ocular manifestations - Q87.42 Marfan syndrome with ocular manifestations
- skeletal manifestations - Q87.43 Marfan syndrome with skeletal manifestation
- cardiovascular manifestations - Q87.418 Marfan 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
- MED13L (mediator complex subunit 13L) - Q87.85 MED13L syndrome
- median arcuate ligament - I77.4 Celiac artery compression syndrome
- mediator complex subunit 13L (MED13L) - Q87.85 MED13L 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 - E88.810 Metabolic syndrome
- metastatic carcinoid - E34.00 Carcinoid syndrome, unspecified
- 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;
- specified type NEC with diffuse membranous glomerulonephritis - N04.29 Other nephrotic syndrome with diffuse membranous glomerulonephritis
- 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 - N04.20 Nephrotic syndrome with diffuse membranous glomerulonephritis, unspecified
- 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
- obliterans
- bronchiolitis - See Also: Bronchiolitis, obliterative; - J44.81 Bronchiolitis obliterans and bronchiolitis obliterans syndrome
- oculomotor - H51.9 Unspecified disorder of binocular movement
- Ogilvie - K59.81 Ogilvie syndrome
- Oliver-McFarlane - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
- 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) - See Also: Syndrome, thoracic outlet; - 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
- Phelan-McDermid - Q93.52 Phelan-McDermid 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 hamartoma 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.C Parkinsonism, unspecified
- 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
- restrictive allograft - J4A.0 Restrictive allograft syndrome
- retinoblastoma (familial) - C69.2 Malignant neoplasm of retina
- retroperitoneal fibrosis - K68.2 Retroperitoneal fibrosis
- 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 - F20.9 Schizophrenia, unspecified
- Schnitzler - D47.2 Monoclonal gammopathy
- Scholte's - E34.09 Other carcinoid syndrome
- Schroeder's - E27.0 Other adrenocortical overactivity
- Schüller-Christian - C96.5 Multifocal and unisystemic Langerhans-cell histiocytosis
- Schwachman (-Diamond) - D61.02 Shwachman-Diamond syndrome
- 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
- serotonin - G90.81 Serotonin 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 (-Diamond) - D61.02 Shwachman-Diamond syndrome
- 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 - I20.89 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
- Snyder-Robinson - Q87.89 Other specified congenital malformation syndromes, not elsewhere classified
- 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 - E34.09 Other 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
- wasting (syndrome) due to underlying condition - E88.A Wasting disease (syndrome) due to underlying condition
- 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
Applicable Clinical Terms Definitions
Ataxia Telangiectasia: An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23).
Basilar Artery: The artery formed by the union of the right and left vertebral arteries; it runs from the lower to the upper border of the pons, where it bifurcates into the two posterior cerebral arteries.
Brachial Plexus: The large network of nerve fibers which distributes the innervation of the upper extremity. The brachial plexus extends from the neck into the axilla. In humans, the nerves of the plexus usually originate from the lower cervical and the first thoracic spinal cord segments (C5-C8 and T1), but variations are not uncommon.
Bronchiolitis Obliterans: Inflammation of the BRONCHIOLES leading to an obstructive lung disease. Bronchioles are characterized by fibrous granulation tissue with bronchial exudates in the lumens. Clinical features include a nonproductive cough and DYSPNEA.
Dyspnea, Paroxysmal: A disorder characterized by sudden attacks of respiratory distress in at rest patients with HEART FAILURE and PULMONARY EDEMA. It usually occurs at night after several hours of sleep in a reclining position. Patients awaken with a feeling of suffocation, coughing, a cold sweat, and TACHYCARDIA. When there is significant WHEEZING, it is called CARDIAC ASTHMA.
Cauda Equina: The lower part of the SPINAL CORD consisting of the lumbar, sacral, and coccygeal nerve roots.
Causalgia: A complex regional pain syndrome characterized by burning pain and marked sensitivity to touch (HYPERESTHESIA) in the distribution of an injured peripheral nerve. Autonomic dysfunction in the form of sudomotor (i.e., sympathetic innervation to sweat glands), vasomotor, and trophic skin changes may also occur. (Adams et al., Principles of Neurology, 6th ed, p1359)
Fees and Charges: Amounts charged to the patient as payer for health care services.
Cluster Headache: A primary headache disorder that is characterized by severe, strictly unilateral PAIN which is orbital, supraorbital, temporal or in any combination of these sites, lasting 15-180 min. occurring 1 to 8 times a day. The attacks are associated with one or more of the following, all of which are ipsilateral: conjunctival injection, lacrimation, nasal congestion, rhinorrhea, facial SWEATING, eyelid EDEMA, and miosis. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
Connective Tissue: Tissue that supports and binds other tissues. It consists of CONNECTIVE TISSUE CELLS embedded in a large amount of EXTRACELLULAR MATRIX.
Croup: Inflammation involving the GLOTTIS or VOCAL CORDS and the subglottic larynx. Croup is characterized by a barking cough, HOARSENESS, and persistent inspiratory STRIDOR (a high-pitched breathing sound). It occurs chiefly in infants and children.
Fatigue: The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli.
Foramen Magnum: The large hole at the base of the skull through which the SPINAL CORD passes.
Frontal Lobe: The part of the cerebral hemisphere anterior to the central sulcus, and anterior and superior to the lateral sulcus.
Glass: Hard, amorphous, brittle, inorganic, usually transparent, polymerous silicate of basic oxides, usually potassium or sodium. It is used in the form of hard sheets, vessels, tubing, fibers, ceramics, beads, etc.
Hypernatremia: Excessive amount of sodium in the blood. (Dorland, 27th ed)
Hyperventilation: A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide.
Hypopituitarism: Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions.
Infant: A child between 1 and 23 months of age.
Vena Cava, Inferior: The venous trunk which receives blood from the lower extremities and from the pelvic and abdominal organs.
Insulin Resistance: Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS.
Jet Lag Syndrome: A chronobiologic disorder resulting from rapid travel across a number of time zones, characterized by insomnia or hypersomnolence, fatigue, behavioral symptoms, headaches, and gastrointestinal disturbances. (From Cooper, Sleep, 1994, pp593-8)
Macrophage Activation: The process of altering the morphology and functional activity of macrophages so that they become avidly phagocytic. It is initiated by lymphokines, such as the macrophage activation factor (MAF) and the macrophage migration-inhibitory factor (MMIF), immune complexes, C3b, and various peptides, polysaccharides, and immunologic adjuvants.
Mandibulofacial Dysostosis: A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by a slant of the palpebral fissures, COLOBOMA of the lower lid, MICROGNATHIA and hypoplasia of the ZYGOMATIC ARCHES, and CONGENITAL MICROTIA. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)
MELAS Syndrome: A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)
Migraine Disorders: A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
Otolithic Membrane: A gelatinous membrane overlying the acoustic maculae of SACCULE AND UTRICLE. It contains minute crystalline particles (otoliths) of CALCIUM CARBONATE and protein on its outer surface. In response to head movement, the otoliths shift causing distortion of the vestibular hair cells which transduce nerve signals to the BRAIN for interpretation of equilibrium.
Ovary: The reproductive organ (GONADS) in female animals. In vertebrates, the ovary contains two functional parts: the OVARIAN FOLLICLE for the production of female germ cells (OOGENESIS); and the endocrine cells (GRANULOSA CELLS; THECA CELLS; and LUTEAL CELLS) for the production of ESTROGENS and PROGESTERONE.
Pain: An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS.
Peptic Ulcer: Ulcer that occurs in the regions of the GASTROINTESTINAL TRACT which come into contact with GASTRIC JUICE containing PEPSIN and GASTRIC ACID. It occurs when there are defects in the MUCOSA barrier. The common forms of peptic ulcers are associated with HELICOBACTER PYLORI and the consumption of nonsteroidal anti-inflammatory drugs (NSAIDS).
Restless Legs Syndrome: A disorder characterized by aching or burning sensations in the lower and rarely the upper extremities that occur prior to sleep or may awaken the patient from sleep.
Serotonin: A biochemical messenger and regulator, synthesized from the essential amino acid L-TRYPTOPHAN. In humans it is found primarily in the central nervous system, gastrointestinal tract, and blood platelets. Serotonin mediates several important physiological functions including neurotransmission, gastrointestinal motility, hemostasis, and cardiovascular integrity. Multiple receptor families (RECEPTORS, SEROTONIN) explain the broad physiological actions and distribution of this biochemical mediator.
Subclavian Steal Syndrome: A clinically significant reduction in blood supply to the BRAIN STEM and CEREBELLUM (i.e., VERTEBROBASILAR INSUFFICIENCY) resulting from reversal of blood flow through the VERTEBRAL ARTERY from occlusion or stenosis of the proximal subclavian or brachiocephalic artery. Common symptoms include VERTIGO; SYNCOPE; and INTERMITTENT CLAUDICATION of the involved upper extremity. Subclavian steal may also occur in asymptomatic individuals. (From J Cardiovasc Surg 1994;35(1):11-4; Acta Neurol Scand 1994;90(3):174-8)
Tourniquets: Devices for the compression of a blood vessel by application around an extremity to control the circulation and prevent the flow of blood to or from the distal area. (From Dorland, 28th ed)
Trisomy: The possession of a third chromosome of any one type in an otherwise diploid cell.
Viruses: Minute infectious agents whose genomes are composed of DNA or RNA, but not both. They are characterized by a lack of independent metabolism and the inability to replicate outside living host cells.
Zellweger Syndrome: An autosomal recessive disorder due to defects in PEROXISOME biogenesis which involves more than 13 genes encoding peroxin proteins of the peroxisomal membrane and matrix. Zellweger syndrome is typically seen in the neonatal period with features such as dysmorphic skull; MUSCLE HYPOTONIA; SENSORINEURAL HEARING LOSS; visual compromise; SEIZURES; progressive degeneration of the KIDNEYS and the LIVER. Zellweger-like syndrome refers to phenotypes resembling the neonatal Zellweger syndrome but seen in children or adults with apparently intact peroxisome biogenesis.
