ZFIN Human Disease: autosomal dominant dyskeratosis congenita 3

OBO ID: DOID:0070018

OBO ID: DOID:0070018

Term Name:	autosomal dominant dyskeratosis congenita 3	Search Ontology:
Synonyms:	DKCA3
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
References:	OMIM:613990
Ontology:	Human Disease ( DOID:0070018 )

Relationships

is a type of:	autosomal dominant disease dyskeratosis congenita autosomal dominant disease dyskeratosis congenita Show first 5 Terms

OTHER autosomal dominant dyskeratosis congenita 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TINF2	tinf2	Dyskeratosis congenita, autosomal dominant 3	613990

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None