OBO ID: DOID:0070020
Term Name: autosomal dominant dyskeratosis congenita 4 Search Ontology:
Synonyms:
  • DKCA4
Definition: A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of the RTEL1 gene on chromosome 20q13.33. https://www.ncbi.nlm.nih.gov/pubmed/23329068
References:
Ontology: Human Disease   ( DOID:0070020 )
Relationships
is a type of:
OTHER autosomal dominant dyskeratosis congenita 4 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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