Cerebellar ataxia and hypergonadotropic hypogonadism

Preferred Label : Cerebellar ataxia and hypergonadotropic hypogonadism;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 605672;

Details

Origin ID

605672;

UMLS CUI

C1854064;

Currated CISMeF NLP mapping
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH concept]
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH Supplementary Concept]
ORDO concept(s)
- Cerebellar ataxia-hypogonadism syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH Supplementary Concept]
- cerebellar ataxia and hypergonadotropic hypogonadism [MeSH concept]
Validated automatic mappings to NTBT
- Cerebellar ataxia-hypogonadism syndrome [ORDO Disease]

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