ZFIN Human Disease: congenital dyserythropoietic anemia type III

OBO ID: DOID:0111399

Term Name:	congenital dyserythropoietic anemia type III		Search Ontology:
Synonyms:	anaemia with multinucleated erythroblasts anemia with multinucleated erythroblasts CDA III CDA type 3 CDA type III CDAN3 Congenital dyserythropoietic anaemia type 3 congenital dyserythropoietic anaemia type III Congenital dyserythropoietic anemia type 3 hereditary benign erythroreticulosis
Definition:	A congenital dyserythropoietic anemia characterized by nonprogressive mild to moderate anemia, macrocytosis in the peripheral blood, and giant multinucleated erythroblasts that has_material_basis_in heterozygous mutation in an 11 cM interval within chromosome 15q21-q25. https://www.ncbi.nlm.nih.gov/pubmed/7711721
References:	GARD:2002 MESH:D000742 OMIM:105600 ORDO:98870 SNOMEDCT_US_2023_03_01:26409005 UMLS_CUI:C0271934
Ontology:	Human Disease ( DOID:0111399 )

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is a type of:	congenital dyserythropoietic anemia congenital dyserythropoietic anemia Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KIF23	kif23	Anemia, congenital dyserythropoietic, type IIIA	105600

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None