Cowden syndrome 2

Preferred Label : Cowden syndrome 2;

Obsolete resource : true;

Moved to : 158350;

Symbol : CWS2;

CISMeF acronym : CWS2;

Type : Phenotype, molecular basis known;

Prefixed ID : 612359;

Details

Origin ID

612359;

UMLS CUI

C3552552;

Currated CISMeF NLP mapping
- Cowden-Like syndrome [MeSH concept]
- Cowden-Like syndrome [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Breast carcinoma [HPO term]
- Endometrial carcinoma [HPO term]
- Papillary thyroid carcinoma [HPO term]
- Uterine leiomyoma [HPO term]
ORDO concept(s)
- Cowden syndrome [ORDO Disease]
See also inter- (CISMeF)
- Cowden like syndrome [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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