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Intrahepatic cholestasis of pregnancy
2 OMIM references -
4 associated genes
14 connected diseases
No signs/symptoms info
Disease Type of connection
Benign recurrent intrahepatic cholestasis type 1
Benign recurrent intrahepatic cholestasis type 2
Low phospholipid associated cholelithiasis
Progressive familial intrahepatic cholestasis type 1
Progressive familial intrahepatic cholestasis type 2
Progressive familial intrahepatic cholestasis type 3
Kostmann syndrome
Amyotrophic lateral sclerosis
Autoimmune lymphoproliferative syndrome with recurrent infections
Estrogen resistance syndrome
Severe combined immunodeficiency due to DNA-PKcs deficiency
Anaplastic ependymoma
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Synonym(s):
- Gravidic intrahepatic cholestasis
- Pregnancy-related cholestasis
- Recurrent intrahepatic cholestasis of pregnancy

Classification (Orphanet):
- Rare gynecologic or obstetric disease
- Rare hepatic disease

Classification (ICD10):
- Pregnancy, childbirth and the puerperium -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
2 OMIM references -
1 MeSH reference: C535932

Gene symbol UniProt reference OMIM reference
ABCB11 O95342603201
ABCB4 P21439171060
ATP8B1 O43520602397
NR1H4 Q96RI1603826
No signs/symptoms info available.