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Hemochromatosis, juvenile, digenic

MedGen UID:: 462212
•Concept ID:: C3150862
•: Finding

Synonym:	HEMOCHROMATOSIS, JUVENILE, DIGENIC

OMIM®:	606464

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PubMed

HAMP as a modifier gene that increases the phenotypic expression of the HFE pC282Y homozygous genotype.

Jacolot S, Le Gac G, Scotet V, Quere I, Mura C, Ferec C
Blood 2004 Apr 1;103(7):2835-40. Epub 2003 Dec 11 doi: 10.1182/blood-2003-10-3366. PMID: 14670915

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Hemochromatosis, juvenile, digenic
Hemochromatosis, juvenile, digenic

MedGen
C3150862[conceptid] (1)
MedGen
C1851316[trait identifier] AND "OMIM"[submitter] (1)
ClinVar
C1853733[trait identifier] AND "OMIM"[submitter] (9)
ClinVar
C1858664[trait identifier] AND "OMIM"[submitter] (5)
ClinVar

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