Fanconi anemia complementation group R
Fanconi anemia that has material basis in heterozygous mutation in the RAD51 gene on chromosome 15q15
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Fanconi anemia complementation group R
Summary
Fanconi anemia complementation group R is a developmental defect during embryogenesis[1].
Key Facts
- Fanconi anemia complementation group R's instance of is recorded as developmental defect during embryogenesis[2].
- Fanconi anemia complementation group R's instance of is recorded as rare disease[3].
- Fanconi anemia complementation group R's instance of is recorded as class of disease[4].
- Fanconi anemia complementation group R's subclass of is recorded as Fanconi anemia[5].
- Fanconi anemia complementation group R's subclass of is recorded as genetic disease[6].
- Fanconi anemia complementation group R's subclass of is recorded as autosomal dominant disease[7].
- Fanconi anemia complementation group R's OMIM ID is recorded as 617244[8].
- Fanconi anemia complementation group R's Disease Ontology ID is recorded as DOID:0111090[9].
- Fanconi anemia complementation group R's genetic association is recorded as RAD51[10].
- Fanconi anemia complementation group R's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111090[11].
- Fanconi anemia complementation group R's exact match is recorded as http://identifiers.org/doid/DOID:0111090[12].
- Fanconi anemia complementation group R's UMLS CUI is recorded as C4284093[13].
- Fanconi anemia complementation group R's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Fanconi anemia complementation group R's Mondo ID is recorded as MONDO_0014986[15].
- Fanconi anemia complementation group R's UniProt disease ID is recorded as DI-04906[16].