About   Help   FAQ
Disease Ontology Browser
hemolytic disease of the fetus (DOID:1098)
Alliance: disease page
Synonyms: alloimmune HDFN; EF - Erythroblastosis foetalis; erythroblastosis fetalis; fetal erythroblastosis; Haemolytic disease due to rhesus isoimmunisation; Hemolytic disease of the fetus and newborn; rhesus isoimmunisation of the newborn
Alt IDs: ICD10CM:P55, ICD9CM:773, ICD9CM:773.2, MESH:D004899, NCI:C101304, UMLS_CUI:C0014761
Definition: A microcytic anemia that is characterized by Rho(D) incompatibility, which may develop when a woman with Rh-negative blood is impregnated by an individual with Rh-positive blood and conceives a fetus with Rh-positive blood, sometimes resulting in hemolysis.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory