Search Ontology:
Human Disease

autosomal dominant dyskeratosis congenita 6

Term ID
DOID:0070023
Synonyms
  • DKCA6
Definition
A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of ACD on chromosome 16q22.1. https://www.ncbi.nlm.nih.gov/pubmed/25205116
References
Ontology
Human Disease   ( DOID:0070023 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models