Fanconi anemia complementation group O
Fanconi anemia that has material basis in homozygous mutation in the RAD51C gene on chromosome 17q21-q24
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Fanconi anemia complementation group O
Summary
Fanconi anemia complementation group O is a developmental defect during embryogenesis[1].
Key Facts
- Fanconi anemia complementation group O's instance of is recorded as developmental defect during embryogenesis[2].
- Fanconi anemia complementation group O's instance of is recorded as rare disease[3].
- Fanconi anemia complementation group O's instance of is recorded as class of disease[4].
- Fanconi anemia complementation group O's subclass of is recorded as Fanconi anemia[5].
- Fanconi anemia complementation group O's subclass of is recorded as genetic disease[6].
- Fanconi anemia complementation group O's subclass of is recorded as autosomal recessive disease[7].
- Fanconi anemia complementation group O's OMIM ID is recorded as 613390[8].
- Fanconi anemia complementation group O's Disease Ontology ID is recorded as DOID:0111096[9].
- Fanconi anemia complementation group O's genetic association is recorded as RAD51C[10].
- Fanconi anemia complementation group O's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111096[11].
- Fanconi anemia complementation group O's exact match is recorded as http://identifiers.org/doid/DOID:0111096[12].
- Fanconi anemia complementation group O's UMLS CUI is recorded as C3150653[13].
- Fanconi anemia complementation group O's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Fanconi anemia complementation group O's Mondo ID is recorded as MONDO_0013248[15].
- Fanconi anemia complementation group O's UniProt disease ID is recorded as DI-02852[16].