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DOID:0050641 - Rh deficiency syndrome
Disease Ontology 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.
Synonyms:
Xenbase Genes : rhd, rhag, rhagl
MONDO:0019107 - Rh deficiency syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hemolytic anemia (is_a)