Search Ontology:
Human Disease
autosomal recessive dyskeratosis congenita 3
- Term ID
- DOID:0070019
- Synonyms
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- DKCB3
- Definition
- A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the WRAP53 gene on chromosome 17p13.1. https://www.ncbi.nlm.nih.gov/pubmed/21205863
- References
- Ontology
- Human Disease ( DOID:0070019 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models