Disease #00357 (HFE2A (hemochromatosis, juvenile, type 2A (HFE-2A)), OMIM:602390)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	HFE2A
Name	hemochromatosis, juvenile, type 2A (HFE-2A)
OMIM ID	602390
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HFE2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-03-17 15:26:25 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.