Cowden syndrome 3

Preferred Label : Cowden syndrome 3;

Obsolete resource : true;

Moved to : 158350;

Symbol : CWS3;

CISMeF acronym : CWS3;

Type : Phenotype, molecular basis known;

Prefixed ID : 615106;

Details

Origin ID

615106;

UMLS CUI

C3554516;

Automatic exact mappings (from CISMeF team)
- SDHD wt Allele [NCIt concept]
ORDO concept(s)
- Cowden syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients