Watson syndrome

Watson syndrome
Classification and external resources
Specialty	Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value).
ICD-10	Q87.1
OMIM	193520
DiseasesDB	32244
Patient UK	Watson syndrome
MeSH	D009456
	[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).\|edit on Wikidata]]]

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.^[1]

Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.^[2]

References

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v t e Phakomatosis (Q85, 759.5–759.6)
Neurofibromatosis	Type I Type II
Angiomatosis	Sturge–Weber syndrome Von Hippel–Lindau disease
Hamartoma	Tuberous sclerosis Hypothalamic hamartoma (Pallister–Hall syndrome) Multiple hamartoma syndrome Proteus syndrome Cowden syndrome Bannayan–Riley–Ruvalcaba syndrome Lhermitte–Duclos disease
Other	Abdallat–Davis–Farrage syndrome Ataxia telangiectasia Incontinentia pigmenti Peutz–Jeghers syndrome

Watson syndrome
Classification and external resources
Specialty	Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value).
ICD-10	Q87.1
OMIM	193520
DiseasesDB	32244
Patient UK	Watson syndrome
MeSH	D009456
[[[d:Lua error in Module:Wikidata at line 863: attempt to index field 'wikibase' (a nil value).\|edit on Wikidata]]]