Watson syndrome https://rarediseases.info.nih.gov/diseases/5540/watson-syndrome https://www.malacards.org/card/watson_syndrome ICD9:709.8 icd11.foundation:1674178232 MEDGEN:107817 pulmonic stenosis with cafe-Au-lait Spots Watson syndrome is believed to be a variant of neurofibromatosis type 1. The symptoms of this condition are pulmonary valvular stenosis, cafe-au-lait spots and short stature. IQTest scores for individuals with Watson syndromecan rangebetween 60-100.Many people with this condition also have a larger than average head size (macrocephaly) and Lisch nodules. While mutations in the NF1 gene have been found in families with Watson syndrome, the exactcause of this condition is unknown. The conditionis inherited in an autosomal dominant pattern. Treatment aims at managing the specific symptoms of an individual. Orphanet:3444 MONDO:0008672 GARD:0005540 UMLS:C0553586 DOID:0070483 WTSN SCTID:403820003 Watson syndrome OMIM:193520 cafe-Au-lait Spots with pulmonic stenosis neurofibromatosis-Noonan syndrome