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Metadata
ID	DOID:0070018
Name	autosomal dominant dyskeratosis congenita 3
Definition	A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of the TINF2 gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/18252230
Xrefs	MIM:613990
Synonyms	DKCA3 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a dyskeratosis congenita
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance