Term Name: autosomal dominant dyskeratosis congenita 3
Synonyms: DKCA3
Definition: A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of the TINF2 gene on chromosome 14q12.
Ontology: Human Disease [DOID:0070018]   ( DOID:0070018 )

Relationships
is a type of: autosomal dominant disease dyskeratosis congenita