Disease #02395 (PFIC2 (cholestasis, intrahepatic, familial, progressive, type 2 (PFIC-2)), OMIM:601847)
Official abbreviation |
PFIC2 |
Name |
cholestasis, intrahepatic, familial, progressive, type 2 (PFIC-2) |
OMIM ID |
601847 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ABCB11 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|