|  Help  |  About  |  Contact Us

DO Term : hemochromatosis type 2 [DOID:0111034] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • GARD:10092,
  • ORDO:79230,
  • MESH:C537247,
  • juvenile hemochromatosis,
  • HFE2,
  • ICD10CM:E83.1,
  • JHH
Quick Links:
 
Quick Links:
 

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents