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Metadata
ID	DOID:0050660
Name	Beare-Stevenson cutis gyrata syndrome
Definition	A syndrome that is characterized by cutis gyrata, acanthosis nigricans and craniosynostosis, has_material_basis_in heterozygous mutation in the FGFR2 gene on chromosome 10q26. https://rarediseases.info.nih.gov/diseases/332/beare-stevenson-cutis-gyrata-syndrome
Xrefs	GARD:332 OMIM:123790
Subsets	DO_rare_slim
Parent Relationships	is_a syndrome is_a autosomal dominant disease