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Summary Literature (0)
DOID:0081113 - Baraitser-Winter syndrome 2

Disease Ontology Definition:A Baraitser-Winter syndrome that has_material_basis_in heterozygous mutation in the ACTG1 gene on chromosome 17q25.

Synonyms:

Xenbase Genes : actg1


MIM:
MIM:614583 - BARAITSER-WINTER SYNDROME 2; BRWS2

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

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