Fanconi anemia complementation group Q
Fanconi anemia that has material basis in compound heterozygous mutation in the ERCC4 gene on chromosome 16p13
Press Enter · cited answer in seconds
0 sources
Fanconi anemia complementation group Q
Summary
Fanconi anemia complementation group Q is a developmental defect during embryogenesis[1].
Key Facts
- Fanconi anemia complementation group Q's instance of is recorded as developmental defect during embryogenesis[2].
- Fanconi anemia complementation group Q's instance of is recorded as rare disease[3].
- Fanconi anemia complementation group Q's instance of is recorded as class of disease[4].
- Fanconi anemia complementation group Q's subclass of is recorded as Fanconi anemia[5].
- Fanconi anemia complementation group Q's subclass of is recorded as genetic disease[6].
- Fanconi anemia complementation group Q's subclass of is recorded as autosomal recessive disease[7].
- Fanconi anemia complementation group Q's OMIM ID is recorded as 615272[8].
- Fanconi anemia complementation group Q's Disease Ontology ID is recorded as DOID:0111093[9].
- Fanconi anemia complementation group Q's genetic association is recorded as ERCC4[10].
- Fanconi anemia complementation group Q's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111093[11].
- Fanconi anemia complementation group Q's exact match is recorded as http://identifiers.org/doid/DOID:0111093[12].
- Fanconi anemia complementation group Q's UMLS CUI is recorded as C3808988[13].
- Fanconi anemia complementation group Q's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Fanconi anemia complementation group Q's Mondo ID is recorded as MONDO_0014108[15].
- Fanconi anemia complementation group Q's UniProt disease ID is recorded as DI-03812[16].