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Metadata
ID	DOID:0111407
Name	Fraser syndrome 2
Definition	A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FREM2 gene on chromosome 13q13.3. https://www.ncbi.nlm.nih.gov/pubmed/15838507
Xrefs	OMIM:617666
Synonyms	FRASRS2 [EXACT]
Parent Relationships	is_a Fraser syndrome