Syndrome - in the ICD-10-CM Index
Annotation Back-References in the 2025 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
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
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
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
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
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
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.
