Watson syndrome
| Watson syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | medical genetics |
| ICD-10 | Q87.1 |
| OMIM | 193520 |
| DiseasesDB | 32244 |
| MeSH | D009456 |
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.
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