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Summary Literature (0)
DOID:0050660 - Beare-Stevenson cutis gyrata syndrome

Disease Ontology 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.

Synonyms:

Echinobase Genes :


MIM:
MIM:123790 - beare-stevenson cutis gyrata syndrome; bstvs

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)