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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

MIM:603467

Synonyms

FANCF [EXACT]

Parent Relationships

is_a monogenic disease

is_a Fanconi anemia

Subclass Logical Relationships

disease has basis in some gene

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