Modifier, X-linked, for neurofunctional defects

Preferred Label : Modifier, X-linked, for neurofunctional defects;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Tourette syndrome, modifier of;

Inheritance : X-linked;

Prefixed ID : 309840;

Details

Origin ID

309840;

UMLS CUI

C1839708;

Currated CISMeF NLP mapping
- modifier, X-Linked, for neurofunctional defects [MeSH concept]
- modifier, X-Linked, for neurofunctional defects [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the nervous system [HPO term]
- X-linked inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- modifier, X-Linked, for neurofunctional defects [MeSH Supplementary Concept]
- modifier, X-Linked, for neurofunctional defects [MeSH concept]

Keyword's position in hierarchy(ies) :

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