OBO ID: DOID:0111034
Term Name: hemochromatosis type 2 Search Ontology:
Synonyms:
  • HFE2
  • JHH
  • juvenile hemochromatosis
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. (2)
References:
Ontology: Human Disease   ( DOID:0111034 )
Relationships
is a type of:
has subtype:
OTHER hemochromatosis type 2 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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