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Low phospholipid associated cholelithiasis
1 OMIM reference -
1 associated gene
3 connected diseases
No signs/symptoms info
Disease Type of connection
Intrahepatic cholestasis of pregnancy
Progressive familial intrahepatic cholestasis type 3
Kostmann syndrome
Synonym(s):
- ABCB4 gene mutation-associated cholelithiasis
- Cholelithiasis with ABCB4 gene mutation
Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ABCB4 P21439171060
No signs/symptoms info available.