congenital dyserythropoietic anemia
Go to external page http://purl.obolibrary.org/obo/MONDO_0019403
Congenital dyserythropoietic anemia (CDA) is a heterogenous group of hematological disorders of late erythropoiesis and red cell abnormalities that lead to anemia. Five types of CDA are defined: CDA I, CDA II, CDA III, CDA IV and thrombocytopenia with CDA. [ Orphanet:85 ]
Synonyms: CDA congenital dyshaematopoietic anemia congenital dyshaematopoietic anaemia anemia, congenital dyserythropoietic
Term information
- DOID:1338 (MONDO:equivalentTo)
- GARD:1999 (MONDO:GARD)
- Orphanet:85 (MONDO:equivalentTo)
- NCIT:C84646 (MONDO:equivalentTo)
- ICD9:285.8 (MONDO:relatedTo)
- MEDGEN:8064 (MONDO:equivalentTo)
- MESH:D000742 (Orphanet:85/e)
- ICD10CM:D64.4 (Orphanet:85/specific)
- icd11.foundation:899830967 (https://orcid.org/0000-0002-4142-7153)
- NANDO:1200885 (https://orcid.org/0000-0003-0011-764X)
- NANDO:2100178 (https://orcid.org/0000-0003-0011-764X)
- UMLS:C0002876 (MONDO:equivalentTo)
- OMIMPS:224120 (https://orcid.org/0000-0002-6601-2165)
- NANDO:2200615 (https://orcid.org/0000-0003-0011-764X)
- SCTID:52951008 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_txgnn_grouping_anemia, mondo_top_grouping_hematologic_disorder, disease_grouping, 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_included, nord_rare, matrix_llm__anatomical_other, icd10_billable, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, harrisons_view_hematologic_disorder, rare, harrisons_view_member, harrisons_view_hereditary_disease, ordo_group_of_disorders
https://omim.org/phenotypicSeries/PS224120
http://purl.bioontology.org/ontology/ICD10CM/D64.4
http://identifiers.org/snomedct/52951008
http://purl.obolibrary.org/obo/NCIT_C84646
http://identifiers.org/medgen/8064
http://linkedlifedata.com/resource/umls/id/C0002876
http://www.orpha.net/ORDO/Orphanet_85
http://purl.obolibrary.org/obo/DOID_1338
http://identifiers.org/mesh/D000742
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/899830967