Metadata | |
---|---|
ID | DOID:0111088 |
Name | Fanconi anemia complementation group F |
Definition | A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/10615118 |
Xrefs | |
Synonyms |
FANCF [EXACT] |
Parent Relationships |
is_a Fanconi anemia is_a monogenic disease |
Subclass Logical Relationships |
disease has basis in some gene |