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General Information
ZIRC
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 TINF2 on chromosome 14q12.https://www.ncbi.nlm.nih.gov/pubmed/18252230
References:
Ontology: Human Disease   (DOID:0070018)
OTHER autosomal dominant dyskeratosis congenita 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TINF2 Dyskeratosis congenita, autosomal dominant 3 613990
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None