Devriendt syndrome

Preferred Label : Devriendt syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 610136;

Origin ID

610136;

UMLS CUI

C1857830;

Currated CISMeF NLP mapping
- Devriendt syndrome [MeSH concept]
- devriendt syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Devriendt syndrome [MeSH concept]
- devriendt syndrome [MeSH Supplementary Concept]