Fanconi anemia complementation group D2
Fanconi anemia that has material basis in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25
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Summary
Fanconi anemia complementation group D2 is a developmental defect during embryogenesis[1]. It is known by 9 alternative names across languages and contexts.[2]
Key Facts
- Fanconi anemia complementation group D2's instance of is recorded as developmental defect during embryogenesis[3].
- Fanconi anemia complementation group D2's instance of is recorded as rare disease[4].
- Fanconi anemia complementation group D2's instance of is recorded as class of disease[5].
- Fanconi anemia complementation group D2 is a type of Fanconi anemia[6].
- Fanconi anemia complementation group D2 is a type of genetic disease[7].
- Fanconi anemia complementation group D2 is a type of autosomal recessive disease[8].
- Fanconi anemia complementation group D2's NCI Thesaurus ID is recorded as C125706[9].
- Fanconi anemia complementation group D2's genetic association is recorded as FANCD2[10].
- Fanconi anemia complementation group D2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111083[11].
- Fanconi anemia complementation group D2's exact match is recorded as http://identifiers.org/doid/DOID:0111083[12].
- Fanconi anemia complementation group D2's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
Why It Matters
Fanconi anemia complementation group D2 is known by 9 alternative names across languages and contexts.[2]