Cholestatic liver disease
Symptom Information:
Symptom ID: | HPO:0002611 | |||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||
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) Cholestatic liver disease(HPO:0002611) MedDRA: Hepatobiliary disorders(MedDRA:10019805) Bile duct disorders(MedDRA:10004606) Obstructive bile duct disorders (excl neoplasms)(MedDRA:10029976) Cholestatic liver disease(HPO:0002611) Hepatic and hepatobiliary disorders(MedDRA:10019654) Cholestasis and jaundice(MedDRA:10008636) Cholestatic liver disease(HPO:0002611) |
|||||||||||||||||||||||||||||||||||||||||||
Database Frequency: | 19 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Bifunctional enzyme deficiency | (Orphanet:300) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Leprechaunism | (Orphanet:508) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Menkes disease | (Orphanet:565) |
NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE | (OMIM:602114) |
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys | (Orphanet:79118) |
Neonatal hemochromatosis | (Orphanet:446) |
Niemann-Pick disease type C | (Orphanet:646) |
Primary sclerosing cholangitis | (Orphanet:171) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Reticular dysgenesis | (Orphanet:33355) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |