Fanconi anemia complementation group T
Fanconi anemia that has material basis in compound heterozygous mutation in the UBE2T gene on chromosome 1q32
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Fanconi anemia complementation group T
Summary
Fanconi anemia complementation group T is a developmental defect during embryogenesis[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- Fanconi anemia complementation group T's instance of is recorded as developmental defect during embryogenesis[3].
- Fanconi anemia complementation group T's instance of is recorded as rare disease[4].
- Fanconi anemia complementation group T's instance of is recorded as class of disease[5].
- Fanconi anemia complementation group T is a type of Fanconi anemia[6].
- Fanconi anemia complementation group T is a type of genetic disease[7].
- Fanconi anemia complementation group T is a type of autosomal recessive disease[8].
- Fanconi anemia complementation group T's genetic association is recorded as UBE2T[9].
- Fanconi anemia complementation group T's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111081[10].
- Fanconi anemia complementation group T's exact match is recorded as http://identifiers.org/doid/DOID:0111081[11].
- Fanconi anemia complementation group T's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
Fanconi anemia complementation group T is known by 6 alternative names across languages and contexts.[2]