Visualize Submit Comment
Metadata
ID DOID:0111085
Name Fanconi anemia complementation group U
Definition A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36.
https://www.ncbi.nlm.nih.gov/pubmed/22232082
Xrefs

OMIM:617247

Synonyms

FANCU [EXACT]

Parent Relationships

is_a Fanconi anemia

is_a autosomal recessive disease

Add an item to the term tracker