Disease #02701 (Hypercholanemia, familial, OMIM:607748)

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Official abbreviation	-
Name	Hypercholanemia, familial
OMIM ID	607748
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	BAAT, EPHX1, TJP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A