striatonigral degeneration, infantile, mitochondrial - CISMeF

" /> striatonigral degeneration, infantile, mitochondrial - CISMeF

CISMeF

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Striatonigral degeneration, infantile, mitochondrialMeSH concept

Preferred Label : striatonigral degeneration, infantile, mitochondrial;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0564325;

UMLS CUI

C1839022;

Currated CISMeF NLP mapping
- Striatonigral degeneration, infantile, mitochondrial [OMIM Phenotype]
Related record
- striatonigral degeneration, infantile, mitochondrial [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Striatonigral degeneration, infantile, mitochondrial [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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05/05/2025

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