ZFIN Human Disease: congenital dyserythropoietic anemia type Ib

OBO ID: DOID:0111397

Term Name:	congenital dyserythropoietic anemia type Ib		Search Ontology:
Synonyms:	CDA, type Ib CDAN1B
Definition:	A congenital dyserythropoietic anemia type I that has_material_basis_in homozygous or compound heterozygous mutation in C15orf41 on chromosome 15q14. https://www.ncbi.nlm.nih.gov/pubmed/23716552
References:	MESH:D000742 OMIM:615631 SNOMEDCT_US_2023_03_01:59548005 UMLS_CUI:C0271933
Ontology:	Human Disease ( DOID:0111397 )

Relationships

is a type of:	autosomal recessive disease congenital dyserythropoietic anemia type I autosomal recessive disease congenital dyserythropoietic anemia type I Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
C15orf41	cdin1	Dyserythropoietic anemia, congenital, type Ib	615631

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None