Disease #02056 (Rh-null, regulator type, OMIM:268150)

Official abbreviation -
Name Rh-null, regulator type
OMIM ID 268150
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 1
Associated with 1 gene RHAG
Associated tissues -
Disease features -
Remarks -