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Metadata
ID DOID:0111081
Name Fanconi anemia complementation group T
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
Xrefs

OMIM:616435

Synonyms

FANCT [EXACT]

Parent Relationships

is_a Fanconi anemia

is_a autosomal recessive disease

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