Search Ontology:
Human Disease
Fanconi anemia complementation group T
- Term ID
- DOID:0111081
- Synonyms
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- 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 )
- is a type of
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- inverse disjoint_from
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Genes Involved
Zebrafish Models