Search Ontology:
Human Disease
autosomal recessive dyskeratosis congenita 1
- Term ID
- DOID:0070015
- Synonyms
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- DKCB1
- Definition
- A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the NOLA3 gene on chromosome 15q14. https://www.ncbi.nlm.nih.gov/pubmed/17507419
- References
- Ontology
- Human Disease ( DOID:0070015 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models