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Summary Literature (0)
MIM:607748 - HYPERCHOLANEMIA, FAMILIAL 1; FHCA1

Xenbase Genes: tjp2, baat, ephx1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011905 - obsolete familial hypercholanemia
MONDO:0031446 - hypercholanemia, familial 1