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PBC3
MCID: BLR017
MIFTS: 13
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Biliary Cirrhosis, Primary, 3 (PBC3)
Categories:
Gastrointestinal diseases, Genetic diseases, Immune diseases, Liver diseases, Rare diseases
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MalaCards integrated aliases for Biliary Cirrhosis, Primary, 3:
Classifications:
MalaCards categories:
Global: Rare diseases Genetic diseases Anatomical: Gastrointestinal diseases Liver diseases Immune diseases |
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OMIM :
56
Primary biliary cirrhosis (PBC) is a chronic, progressive cholestatic liver disease that usually affects middle-aged women and eventually leads to liver failure (summary by Kaplan, 1996).
For a discussion of genetic heterogeneity of primary biliary cirrhosis (PBC), see PBC1 (109720). (613008)
MalaCards based summary : Biliary Cirrhosis, Primary, 3, also known as pbc3, is related to primary biliary cirrhosis. An important gene associated with Biliary Cirrhosis, Primary, 3 is PBC3 (Biliary Cirrhosis, Primary, 3). Affiliated tissues include liver. |
Diseases in the Primary Biliary Cirrhosis family:
Diseases related to Biliary Cirrhosis, Primary, 3 via text searches within MalaCards or GeneCards Suite gene sharing:
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MalaCards organs/tissues related to Biliary Cirrhosis, Primary, 3:40
Liver
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Genes related to Biliary Cirrhosis, Primary, 3 (1 elite genes): - Elite gene
- Cancer Census gene in COSMIC
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Search
GEO
for disease gene expression data for Biliary Cirrhosis, Primary, 3.
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