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Human Disease

autosomal recessive dyskeratosis congenita 2

Term ID
DOID:0070017
Synonyms
  • DKCB2
Definition
A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the NOLA2 gene on chromosome 5q35.3. https://www.ncbi.nlm.nih.gov/pubmed/18523010
References
Ontology
Human Disease   ( DOID:0070017 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models