congenital dyserythropoietic anemia type 3
Go to external page http://purl.obolibrary.org/obo/MONDO_0007109
Congenital dyserythropoietic anemia type III (CDA III) is a rare form of CDA characterized by dyserythropoiesis, with big multinucleated erythroblasts in the bone marrow, and manifesting with mild to moderate anemia. [ Orphanet:98870 ]
Synonyms: dyserythropoietic anemia, congenital, type III CDA type 3 CDA III congenital dyserythropoietic anemia type 3 CDA type III
Term information
- Orphanet:98870 (OMIM:105600)
- OMIM:105600 (Orphanet:98870/e)
- ICD9:285.8 (MONDO:relatedTo)
- DOID:0111399 (MONDO:equivalentTo)
- GARD:2002 (MONDO:GARD)
- MEDGEN:1801596 (MONDO:equivalentTo)
- SCTID:26409005 (MONDO:equivalentTo)
- NANDO:1200888 (https://orcid.org/0000-0003-0011-764X)
- UMLS:C5676874 (MONDO:equivalentTo)
gard_rare, ordo_disorder, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, mondo_top_grouping_hematologic_disorder, matrix_txgnn_grouping_anemia, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, matrix_included, matrix_llm__tag_existing_treatment_other, nord_rare, 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, orphanet_rare
http://identifiers.org/snomedct/26409005
http://linkedlifedata.com/resource/umls/id/C5676874
http://identifiers.org/medgen/1801596
http://purl.obolibrary.org/obo/DOID_0111399
https://omim.org/entry/105600
http://www.orpha.net/ORDO/Orphanet_98870
anemia, congenital dyserythropoietic, type III
CDA 3
CDAN3
anemia with multinucleated erythroblasts
dyserythropoietic anemia, congenital type 3
Erythroreticulosis, hereditary benign
anaemia with multinucleated erythroblasts
dyserythropoietic Anemia, congenital, type 3
https://github.com/monarch-initiative/mondo/issues/4069
https://github.com/monarch-initiative/mondo/issues/4521