A hemochromatosis type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the HJV gene on chromosome 1q21. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/14647275 ]

Synonyms: HFE2A

This is just here as a test because I lose it

Term information

acronym
HFE2A

has obo namespace

disease_ontology

id

DOID:0111027