A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. [ NCIT:C34379 ]
Synonyms: congenital hemolytic anaemia hereditary hemolytic anaemia hereditary hemolytic anemia congenital hemolytic anemia
Term information
- NANDO:2100183 (https://orcid.org/0000-0003-0011-764X)
- ICD9:282 (DOID:589)
- NCIT:C34379 (MONDO:equivalentTo)
- UMLS:C0002881 (MONDO:equivalentTo)
- DOID:589 (MONDO:equivalentTo)
- SCTID:42601008 (MONDO:equivalentTo)
- MEDGEN:1919 (MONDO:equivalentTo)
- ICD9:282.9 (DOID:589)
- GARD:6167 (MONDO:GARD)
- MESH:D000745 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_txgnn_grouping_anemia, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_hematologic_disorder, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_hereditary_disease
http://identifiers.org/snomedct/42601008
http://purl.obolibrary.org/obo/NCIT_C34379
http://identifiers.org/medgen/1919
http://purl.obolibrary.org/obo/DOID_589
http://linkedlifedata.com/resource/umls/id/C0002881
http://identifiers.org/mesh/D000745