Fanconi anemia complementation group N
Fanconi anemia that has material basis in compound heterozygous mutation in the PALB2 gene on chromosome 16p12
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Fanconi anemia complementation group N
Summary
Fanconi anemia complementation group N is a developmental defect during embryogenesis[1].
Key Facts
- Fanconi anemia complementation group N's instance of is recorded as developmental defect during embryogenesis[2].
- Fanconi anemia complementation group N's instance of is recorded as rare disease[3].
- Fanconi anemia complementation group N's instance of is recorded as class of disease[4].
- Fanconi anemia complementation group N's subclass of is recorded as Fanconi anemia[5].
- Fanconi anemia complementation group N's subclass of is recorded as genetic disease[6].
- Fanconi anemia complementation group N's subclass of is recorded as monogenic disease[7].
- Fanconi anemia complementation group N's MeSH descriptor ID is recorded as C563657[8].
- Fanconi anemia complementation group N's OMIM ID is recorded as 610832[9].
- Fanconi anemia complementation group N's Disease Ontology ID is recorded as DOID:0111094[10].
- Fanconi anemia complementation group N's NCI Thesaurus ID is recorded as C176894[11].
- Fanconi anemia complementation group N's genetic association is recorded as PALB2[12].
- Fanconi anemia complementation group N's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111094[13].
- Fanconi anemia complementation group N's exact match is recorded as http://identifiers.org/doid/DOID:0111094[14].
- Fanconi anemia complementation group N's UMLS CUI is recorded as C1835817[15].
- Fanconi anemia complementation group N's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- Fanconi anemia complementation group N's Mondo ID is recorded as MONDO_0012565[17].
- Fanconi anemia complementation group N's UniProt disease ID is recorded as DI-01604[18].