watson syndrome

Preferred Label : watson syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0374985;

UMLS CUI

C0553586;

Automatic exact mappings (from CISMeF team)
- Hereditary coproporphyria (disorder) [SNOMED CT concept]
- Watson syndrome [PASCAL descriptor]
- Watson syndrome [ICD-11 More detail]
- hereditary coproporphyria [SNOMED Notion]
CISMeF manual mappings
- pulmonic stenosis with cafe-au-lait spots [Disease (Nov.)]
Currated CISMeF NLP mapping
- Café-au-lait macules with pulmonary stenosis (disorder) [SNOMED CT concept]
- Watson syndrome [OMIM Phenotype]
- Watson syndrome [ORDO Disease]
Related record
- neurofibromatosis 1 [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Café-au-lait macules with pulmonary stenosis (disorder) [SNOMED CT concept]
- Watson syndrome [OMIM Phenotype]
- Watson syndrome [ORDO Disease]
- pulmonic stenosis with cafe-au-lait spots [Disease (Nov.)]