Deafness-Hypogonadism syndrome

Preferred Label : Deafness-Hypogonadism syndrome;

Origin ID

C564435;

UMLS CUI

C1844680;

Automatic exact mappings (from CISMeF team)
- Deafness and hypogonadism syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Deafness-hypogonadism syndrome [OMIM Phenotype]
- Deafness-hypogonadism syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- hearing loss, mixed conductive-sensorineural [MeSH Descriptor]
- hypogonadism [MeSH Descriptor]
Record concept(s)
- Deafness-Hypogonadism syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness and hypogonadism syndrome (disorder) [SNOMED CT concept]
- Deafness-hypogonadism syndrome [OMIM Phenotype]
- Deafness-hypogonadism syndrome [ORDO Disease]