has material basis in germline mutation in ABCB4 progressive familial intrahepatic cholestasis type 3 https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/1289/progressive-familial-intrahepatic-cholestasis-type-3 https://www.malacards.org/card/cholestasis_progressive_familial_intrahepatic_3_2 progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase MESH:C535935 cholestasis, progressive familial intrahepatic 3 NANDO:1201045 icd11.foundation:1276600959 cholestasis, progressive familial intrahepatic, type 3 OMIM:602347 UMLS:C1865643 Progressive familial intrahepatic cholestasis type 3 (PFIC3), a type of progressive familial intrahepatic cholestasis (PFIC), is a late-onset hereditary disorder in bile formation that is hepatocellular in origin. Onset may occur from infancy to young adulthood. MDR3 Deficiency MONDO:0011214 progressive familial intrahepatic cholestasis caused by mutation in ABCB4 DOID:0070223 PFIC3 ABCB4 progressive familial intrahepatic cholestasis cholestasis, progressive familial intrahepatic, 3 MEDGEN:356333 GARD:0001289 NORD:1416 Orphanet:79305 progressive familial intrahepatic cholestasis