Cowden syndrome 4

Preferred Label : Cowden syndrome 4;

Symbol : CWS4;

CISMeF acronym : CWS4;

Type : Phenotype, molecular basis known;

Prefixed ID : #615107;

Details

Origin ID

615107;

UMLS CUI

C3554517;

Currated CISMeF NLP mapping
- Cowden syndrome 4 [DO Concept]
Genes related to phenotype
- Killin [OMIM gene]
HPO term(s)
- Breast carcinoma [HPO term]
- Dysplastic gangliocytoma of the cerebellum [HPO term]
- Hamartoma [HPO term]
- Macrocephaly [HPO term]
- Renal neoplasm [HPO term]
- Trichilemmoma [HPO term]
ORDO concept(s)
- Cowden syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- Cowden syndrome [ORDO Disease]

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