Specialty medical genetics OMIM 193520 MeSH D009456 | ICD-10 Q87.1 DiseasesDB 32244 | |
Watson syndrome is an autosomal dominant condition characterized by Lisch nodules of the ocular iris, axillary/inguinal freckling, pulmonary valvular stenosis, relative macrocephaly, short stature, and neurofibromas.
Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.
References
Watson syndrome Wikipedia(Text) CC BY-SA