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Summary Literature (0)
MIM:613990 - DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3

Xenbase Genes: tinf2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013522 - dyskeratosis congenita, autosomal dominant 3
MONDO:0015780 - dyskeratosis congenita
MONDO:0018045 - Hoyeraal-Hreidarsson syndrome

Disease Ontology (DO):
DOID:0070018 - autosomal dominant dyskeratosis congenita 3