A disorder of the fetus or newborn that occurs when fetal cells that are coated with IgG alloantibodies from the mother attack antigens inherited from the father. Severity can range from absence of symptoms to death. [ NCIT:P378 ]
Synonyms: haemolytic disease due to rhesus isoimmunisation EF - erythroblastosis foetalis erythroblastosis fetalis hemolytic disease of the newborn HDFN hemolytic disease of the foetus or newborn rhesus isoimmunisation of the newborn isoimmune hemolytic disease of the newborn hemolytic disease of the fetus or newborn
Term information
- MESH:D004899 (MONDO:equivalentTo)
- MEDGEN:4530 (MONDO:equivalentTo)
- UMLS:C0014761 (MONDO:equivalentTo)
- ICD9:773.2 (MONDO:relatedTo)
- SCTID:387705004 (MONDO:equivalentTo)
- DOID:1098 (MONDO:equivalentTo)
- EFO:1000937 (MONDO:equivalentTo)
- ICD9:773 (DOID:1098)
- NCIT:C101304 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_txgnn_grouping_anemia, mondo_top_grouping_hematologic_disorder, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, matrix_included, nord_rare, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, matrix_txgnn_grouping_member, rare, harrisons_view_member
http://purl.obolibrary.org/obo/NCIT_C101304
http://identifiers.org/mesh/D004899
http://www.ebi.ac.uk/efo/EFO_1000937
http://identifiers.org/medgen/4530
http://purl.obolibrary.org/obo/DOID_1098
http://identifiers.org/snomedct/387705004
http://linkedlifedata.com/resource/umls/id/C0014761