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Summary Literature (0)
DOID:0070483 - Watson syndrome

Disease Ontology Definition:A RASopathy characterized by pulmonic stenosis, cafe-au-lait macules, decreased intellectual ability, and short stature that has_material_basis_in heterozygous mutation in the NF1 gene on chromosome 17q11.2.

Synonyms:

Xenbase Genes : nf1


MIM:
MIM:193520 - WATSON SYNDROME; WTSN

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), RASopathy (is_a)