bassoe syndrome

Preferred Label : bassoe syndrome;

MeSH note : Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract;

Origin ID

C537661;

UMLS CUI

C2931578;

Automatic exact mappings (from CISMeF team)
- Congenital muscular dystrophy - infantile cataract - hypogonadism [ICD-11 More detail]
Currated CISMeF NLP mapping
- Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- hypogonadism [MeSH Descriptor]
- muscular dystrophies [MeSH Descriptor]
Record concept(s)
- Bassoe syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) [SNOMED CT concept]