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Human Disease

autosomal recessive dyskeratosis congenita 1

Term ID
DOID:0070015
Synonyms
  • 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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models