Search Ontology:
Human Disease

progressive familial intrahepatic cholestasis 3

Term ID
DOID:0070223
Synonyms
  • MDR3 deficiency
  • PFIC3
  • progressive familial intrahepatic cholestasis with elevated serum gama-glutamyltransferase
Definition
A progressive familial intrahepatic cholestasis characterized by autosomal recessive inheritance of intrahepatic cholestasis and elevated serum GGT1 activity that has_material_basis_in mutation in the ABCB4 gene on chromosome 7q21.12. https://www.ncbi.nlm.nih.gov/pubmed/9419367
References
Ontology
Human Disease   ( DOID:0070223 )
Relationships
is a type of
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Genes Involved
Zebrafish Models