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Disease Ontology Browser
hemochromatosis type 2 (DOID:0111034)
Alliance: disease page
Synonyms: HFE2; JHH; juvenile hemochromatosis
Alt IDs: ICD10CM:E83.1, MESH:C537247, ORDO:79230
Definition: A hemochromatosis characterized by autosomal recessive inheritance of early onset of severe iron loading with symptoms including; hypogonadotropic hypogonadism, cardiomyopathy, arthropathy, and liver fibrosis or cirrhosis.

Disease References using Mouse Models (6)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory