Search Ontology:
Human Disease

autosomal recessive dyskeratosis congenita 6

Term ID
DOID:0070024
Synonyms
  • DKCB6
Definition
A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the PARN gene on chromosome 16p13.12. https://www.ncbi.nlm.nih.gov/pubmed/25893599
References
Ontology
Human Disease   ( DOID:0070024 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models