A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12. [ url:https://rarediseases.info.nih.gov/diseases/12916/rh-deficiency-syndrome http://purl.obolibrary.org/obo/ECO_0007637 http://purl.obolibrary.org/obo/ECO_0007645 url:https://www.ncbi.nlm.nih.gov/pubmed/3103426 ]

This is just here as a test because I lose it

Term information

comment

OMIM mapping confirmed by DO. [SN].

definition

A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12.

has obo namespace

disease_ontology

id

DOID:0050641

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