Fanconi anemia complementation group V
Fanconi anemia that has material basis in homozygous mutation in the MAD2L2 gene on chromosome 1p36
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Fanconi anemia complementation group V
Summary
Fanconi anemia complementation group V is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Fanconi anemia complementation group V's instance of is recorded as developmental defect during embryogenesis[3].
- Fanconi anemia complementation group V's instance of is recorded as rare disease[4].
- Fanconi anemia complementation group V's instance of is recorded as class of disease[5].
- Fanconi anemia complementation group V is a type of Fanconi anemia[6].
- Fanconi anemia complementation group V is a type of genetic disease[7].
- Fanconi anemia complementation group V is a type of autosomal recessive disease[8].
- Fanconi anemia complementation group V's genetic association is recorded as MAD2L2[9].
- Fanconi anemia complementation group V's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111080[10].
- Fanconi anemia complementation group V's exact match is recorded as http://identifiers.org/doid/DOID:0111080[11].
- Fanconi anemia complementation group V's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
Fanconi anemia complementation group V is known by 5 alternative names across languages and contexts.[2]