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 is a type of Fanconi anemia[5].
- Fanconi anemia complementation group N is a type of genetic disease[6].
- Fanconi anemia complementation group N is a type of monogenic disease[7].
- Fanconi anemia complementation group N's NCI Thesaurus ID is recorded as C176894[8].
- Fanconi anemia complementation group N's genetic association is recorded as PALB2[9].
- Fanconi anemia complementation group N's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111094[10].
- Fanconi anemia complementation group N's exact match is recorded as http://identifiers.org/doid/DOID:0111094[11].
- Fanconi anemia complementation group N's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].