Hemolytic disease of fetus and newborn, rh-induced

Preferred Label : Hemolytic disease of fetus and newborn, rh-induced;

Symbol : HDFNRH;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Rh disease; Rh fetomaternal incompatibility;

Prefixed ID : #619462;

Details

Origin ID

619462;

UMLS CUI

C0748400;

Genes related to phenotype
- Rhesus blood group, D antigen [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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