raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3444

Watson syndrome

inactive · moved to ORPHA:636Neurofibromatosis type 1

Synonyms: Pulmonic stenosis with 'café-au-lait' spots

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Neurofibromatosis type 1

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enWatson syndromePulmonic stenosis with 'café-au-lait' spots
frSyndrome de WatsonSyndrome de sténose pulmonaire-taches café au lait
deWatson-SyndromLungenstenose mit Café-au-lait Flecken
esSíndrome de WatsonEstenosis pulmonar-manchas café con leche
itSindrome di WatsonStenosi polmonare - macchie caffè-latte
nlSyndroom van WatsonPulmonale stenose met café-au-lait vlekken
ptSíndrome WatsonEstenose pulmonar com manchas 'café com leite'
plZespół WatsonaZwężenie tetnicy płucnej z plamami typu "kawa z mlekiem
csWatsonův syndromPulmonální stenóza se skvrnami "café-au-lait
ukСиндром ВатсонаСтеноз легеневої артерії з плямами кава з молоком
zhWatson综合征肺动脉狭窄伴牛奶咖啡斑
trWatson sendromuCafé-au-lait' lekeli pulmonik stenoz
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM193520Evalidated
UMLSC0553586Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card