lipodystrophy with congenital cataracts and neurodegeneration - CISMeF

" /> lipodystrophy with congenital cataracts and neurodegeneration - CISMeF

CISMeF

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Lipodystrophy with congenital cataracts and neurodegenerationMeSH Supplementary Concept

Preferred Label : lipodystrophy with congenital cataracts and neurodegeneration;

Details

Origin ID

C564669;

UMLS CUI

C1847582;

Currated CISMeF NLP mapping
- Lipodystrophy, familial partial, type 7 [OMIM Phenotype]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- heredodegenerative disorders, nervous system [MeSH Descriptor]
- lipodystrophy, familial partial [MeSH Descriptor]
Record concept(s)
- lipodystrophy with congenital cataracts and neurodegeneration [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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03/01/2026

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