Deafness-hypogonadism syndrome

Preferred Label : Deafness-hypogonadism syndrome;

CISMeF acronym : DHS;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : DHS;

Prefixed ID : 304350;

Détails

Origin ID

304350;

UMLS CUI

C1844680;

Automatic exact mappings (from CISMeF team)
- Deafness - hypogonadism [ICD-11 More detail]
- Deoxyhypusine Synthase [NCIt concept]
- Drug Hypersensitivity Syndrome [NCIt concept]
- diet therapy [MeSH Descriptor]
- xerocytosis, hereditary [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Deafness-Hypogonadism syndrome [MeSH concept]
- Deafness-Hypogonadism syndrome [MeSH Supplementary Concept]
- Deafness-hypogonadism syndrome [ORDO Disease]
ORDO concept(s)
- Deafness-hypogonadism syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Deafness and hypogonadism syndrome (disorder) [SNOMED CT concept]
- Deafness-Hypogonadism syndrome [MeSH Supplementary Concept]
- Deafness-Hypogonadism syndrome [MeSH concept]
- Deafness-hypogonadism syndrome [ORDO Disease]

Position du mot-clé dans l'(les) arborescence(s) :

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