OBO ID: DOID:0111081
Term Name: Fanconi anemia complementation group T Search Ontology:
Synonyms:
  • FANCT
Definition: A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/26046368
References:
Ontology: Human Disease   ( DOID:0111081 )
Relationships
is a type of:
inverse disjoint_from:
OTHER Fanconi anemia complementation group T PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
UBE2T Fanconi anemia, complementation group T 616435
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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