| Disease Browser
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Parent Node:
 Cholestasis (D002779) | Parent Node:
Liver Diseases (D008107) | ..Starting node
.. Cholestasis, Intrahepatic (D002780)
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Child Nodes:
| | ........Alagille Syndrome (D016738) | | ........Bile acid synthesis defect, congenital, 4 (C535444) | | ........CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2 (OMIM:605479) | | ........Cholestasis, progressive familial intrahepatic 1 (C535933) | | ........Cholestasis, progressive familial intrahepatic 2 (C535934) | | ........Cholestasis, progressive familial intrahepatic 3 (C535935) | | ........Intrahepatic Cholestasis of Pregnancy (C535932) | ........Liver Cirrhosis, Biliary (D008105)  5 | | ........Nephropathy, Progressive Tubulointerstitial, with Cholestatic Liver Disease (C566573) |
Sister Nodes: | ..alpha 1-Antitrypsin Deficiency (D019896) 1
| ..Budd-Chiari Syndrome (D006502) 1
| ..Carnitine Palmitoyltransferase II Deficiency, Infantile (C563462)
| ..Cholestasis, Intrahepatic (D002780) 14
| ..COACH syndrome (C536430)
| ..Congenital Hepatic Fibrosis (C580013)
| ..Cyanosis and Hepatic Disease (C565660)
| ..Drug-Induced Liver Injury (D056486) 2
| ..Fatty Liver (D005234) 6
| ..Focal Nodular Hyperplasia (D020518)
| ..Glycogen Storage Disease 0, Liver (C565485)
| ..GSD IV, Nonprogressive Hepatic (C565540)
| ..Hepatic Insufficiency (D048550) 9
| ..Hepatic Veno-Occlusive Disease (D006504) 1
| ..Hepatitis (D006505) 17
| ..Hepatolenticular Degeneration (D006527) 2
| ..Hepatomegaly (D006529) 4
| ..Hepatopulmonary Syndrome (D020065)
| ..Hepatorenal Syndrome (D006530)
| ..Hypertension, Portal (D006975) 3
| ..Liver Abscess (D008100) 2
| ..Liver Cirrhosis (D008103) 16
| ..Liver Diseases, Alcoholic (D008108) 3
| ..Liver Diseases, Parasitic (D008109) 5
| ..Liver Fibrocystic Disease and Polydactyly (C565272)
| ..Liver Neoplasms (D008113) 8
| ..Navajo neurohepatopathy (C538344) 1
| ..Peliosis Hepatis (D010382)
| ..Phosphoenolpyruvate carboxykinase deficiency (C536654)
| ..Polycystic liver disease (C536330)
| ..Porphyrias, Hepatic (D017094) 14
| ..RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
| ..Retinohepatoendocrinologic Syndrome (C564839)
| ..Tuberculosis, Hepatic (D014386)
| ..Zellweger Syndrome (D015211) 3
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 2107 |
| Name: | Cholestasis, Intrahepatic |
| Definition: | Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). |
| Alternative IDs: | |
| ParentIDs: | MESH:D002779|MESH:D008107 |
| TreeNumbers: | C06.130.120.135.250 |C06.552.150 |
| Synonyms: | Bile Duct Obstruction, Intrahepatic |Biliary Stases, Intrahepatic |Biliary Stasis, Intrahepatic |Cholestases, Intrahepatic |Intrahepatic Biliary Stases |Intrahepatic Biliary Stasis |Intrahepatic Cholestases |Intrahepatic Cholestasis |
| Slim Mappings: | Digestive system disease |
| Reference: |
MedGen: D002780
MeSH: D002780
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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