sudden infant death with dysgenesis of the testes syndrome

Preferred Label : sudden infant death with dysgenesis of the testes syndrome;

MeSH note : mutation in TSPYL1;

Origin ID

C563856;

UMLS CUI

C1837371;

Currated CISMeF NLP mapping
- Sudden infant death - dysgenesis of the testes [ICD-11 More detail]
- Sudden infant death with dysgenesis of testes syndrome (disorder) [SNOMED CT concept]
- Sudden infant death with dysgenesis of the testes syndrome [Disease (Nov.)]
- Sudden infant death with dysgenesis of the testes syndrome [OMIM Phenotype]
- Sudden infant death-dysgenesis of the testes syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- sudden infant death [MeSH Descriptor]
- testis [MeSH Descriptor]
Record concept(s)
- sudden infant death with dysgenesis of the testes syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Sudden infant death - dysgenesis of the testes [ICD-11 More detail]
- Sudden infant death with dysgenesis of testes syndrome (disorder) [SNOMED CT concept]
- Sudden infant death with dysgenesis of the testes syndrome [OMIM Phenotype]
- Sudden infant death with dysgenesis of the testes syndrome [Disease (Nov.)]
- Sudden infant death-dysgenesis of the testes syndrome [ORDO Disease]