Cholestasis
Symptom Information:
Symptom ID: | HPO:0001396 | |||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Abnormality of the biliary system(HPO:0004297) Cholestasis(HPO:0001396) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Bile duct disorders(MedDRA:10004606) Obstructive bile duct disorders (excl neoplasms)(MedDRA:10029976) Cholestasis(HPO:0001396) Hepatic and hepatobiliary disorders(MedDRA:10019654) Cholestasis and jaundice(MedDRA:10008636) Cholestasis(HPO:0001396) |
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Database Frequency: | 136 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Adult Still's disease | (Orphanet:829) |
Alagille syndrome | (Orphanet:52) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alagille syndrome due to a NOTCH2 point mutation | (Orphanet:261629) |
Alpha-1-antitrypsin deficiency | (Orphanet:60) |
Alpha-thalassemia | (Orphanet:846) |
Alveolar echinococcosis | (Orphanet:284) |
Apolipoprotein A-I deficiency | (Orphanet:425) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autoimmune hemolytic anemia | (Orphanet:98375) |
Autoimmune hemolytic anemia, warm type | (Orphanet:90033) |
Autosomal agammaglobulinemia | (Orphanet:33110) |
Autosomal dominant beta2-microglobulinic amyloidosis | (Orphanet:314652) |
Babesiosis | (Orphanet:108) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Beta-thalassemia | (Orphanet:848) |
Beta-thalassemia major | (Orphanet:231214) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Budd-Chiari syndrome | (Orphanet:131) |
Carcinoma of the gallbladder | (Orphanet:56044) |
Carney triad | (Orphanet:139411) |
Central congenital hypothyroidism | (Orphanet:226298) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Cholangiocarcinoma | (Orphanet:70567) |
Cholestasis - lymphedema | (Orphanet:1414) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Choreoacanthocytosis | (Orphanet:2388) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Classic galactosemia | (Orphanet:79239) |
Congenital bile acid synthesis defect type 1 | (Orphanet:79301) |
Congenital bile acid synthesis defect type 2 | (Orphanet:79303) |
Congenital bile acid synthesis defect type 3 | (Orphanet:79302) |
Congenital bile acid synthesis defect type 4 | (Orphanet:79095) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital hypothyroidism due to developmental anomaly | (Orphanet:95711) |
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies | (Orphanet:95715) |
Congenital rubella syndrome | (Orphanet:290) |
Congenital toxoplasmosis | (Orphanet:858) |
Crigler-Najjar syndrome | (Orphanet:205) |
Crigler-Najjar syndrome type 1 | (Orphanet:79234) |
Crigler-Najjar syndrome type 2 | (Orphanet:79235) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Disorder of bile acid synthesis | (Orphanet:79168) |
Distomatosis | (Orphanet:1685) |
Dominant beta-thalassemia | (Orphanet:231226) |
Drug rash with eosinophilia and systemic symptoms | (Orphanet:139402) |
Drug-induced autoimmune hemolytic anemia | (Orphanet:90037) |
Dubin-Johnson syndrome | (Orphanet:234) |
Familial renal amyloidosis | (Orphanet:85450) |
Familial thyroid dyshormonogenesis | (Orphanet:95716) |
Fumaric aciduria | (Orphanet:24) |
GRACILE syndrome | (Orphanet:53693) |
Galactose epimerase deficiency | (Orphanet:79238) |
Galactosemia | (Orphanet:352) |
Gastrointestinal stromal tumor | (Orphanet:44890) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Griscelli disease | (Orphanet:381) |
Griscelli disease type 2 | (Orphanet:79477) |
Hashimoto-Pritzker syndrome | (Orphanet:99872) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hydatidosis | (Orphanet:400) |
Hyperbiliverdinemia | (Orphanet:276405) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hypothyroidism due to TSH receptor mutations | (Orphanet:90673) |
Hypothyroidism due to deficient transcription factors involved in pituitary development or function | (Orphanet:226307) |
Ichthyosis - hypotrichosis - sclerosing cholangitis | (Orphanet:59303) |
Idiopathic congenital hypothyroidism | (Orphanet:95717) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated polycystic liver disease | (Orphanet:2924) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
Isolated thyroid-stimulating hormone deficiency | (Orphanet:90674) |
Jeune syndrome | (Orphanet:474) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Kawasaki disease | (Orphanet:2331) |
Klatskin tumor | (Orphanet:99978) |
Lambert syndrome | (Orphanet:1296) |
Lathosterolosis | (Orphanet:46059) |
Legionellosis | (Orphanet:549) |
Leprechaunism | (Orphanet:508) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Lichen planopilaris | (Orphanet:525) |
MEDNIK syndrome | (Orphanet:171851) |
Menkes disease | (Orphanet:565) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Mixed-type autoimmune hemolytic anemia | (Orphanet:90036) |
Mucopolysaccharidosis type 7 | (Orphanet:584) |
Muscular pseudohypertrophy - hypothyroidism | (Orphanet:2349) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys | (Orphanet:79118) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephronophthisis 16 | (OMIM:615382) |
Nephronophthisis 18 | (OMIM:615862) |
Nephronophthisis 19 | (OMIM:616217) |
Nephronophthisis 9 | (OMIM:613824) |
Niemann-Pick disease type C | (Orphanet:646) |
Obesity due to pro-opiomelanocortin deficiency | (Orphanet:71526) |
Occipital horn syndrome | (Orphanet:198) |
Pearson syndrome | (Orphanet:699) |
Peripheral hypothyroidism | (Orphanet:226310) |
Peripheral resistance to thyroid hormones | (Orphanet:97927) |
Permanent congenital hypothyroidism | (Orphanet:226292) |
Polyarteritis nodosa | (Orphanet:767) |
Primary congenital hypothyroidism | (Orphanet:226295) |
Primary congenital hypothyroidism without thyroid developmental anomaly | (Orphanet:95714) |
Progressive familial intrahepatic cholestasis | (Orphanet:172) |
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 | (OMIM:208540) |
Relapsing polychondritis | (Orphanet:728) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |
Renal-hepatic-pancreatic dysplasia | (Orphanet:294415) |
Resistance to thyrotropin-releasing hormone syndrome | (Orphanet:99832) |
Reynolds syndrome | (Orphanet:779) |
Rift valley fever | (Orphanet:319251) |
Rotor syndrome | (Orphanet:3111) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
Senior-Loken syndrome 9 | (OMIM:616629) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Syndromic diarrhea | (Orphanet:84064) |
Thyroid ectopia | (Orphanet:95712) |
Thyroid hemiagenesis | (Orphanet:95719) |
Thyroid hypoplasia | (Orphanet:95720) |
Transient congenital hypothyroidism | (Orphanet:178045) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolman disease | (Orphanet:75233) |
X-linked agammaglobulinemia | (Orphanet:47) |
Yellow fever | (Orphanet:99829) |
Zellweger syndrome | (Orphanet:912) |