Search Ontology:
Human Disease

Fanconi anemia complementation group T

Term ID
DOID:0111081
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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