A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13. [ http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/12469120 ]

Synonyms: HFE2B

This is just here as a test because I lose it

Term information

acronym
HFE2B

has obo namespace

disease_ontology

id

DOID:0111032