retinal cone dystrophy 1 - CISMeF

" /> retinal cone dystrophy 1 - CISMeF

CISMeF

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Retinal cone dystrophy 1MeSH Supplementary Concept

Preferred Label : retinal cone dystrophy 1;

MeSH note : aka RCD1;

MeSH synonym : cone dystrophy, autosomal dominant; retinal cone degeneration;

Details

Origin ID

C566719;

UMLS CUI

C1867326;

Currated CISMeF NLP mapping
- Retinal cone dystrophy 1 [OMIM Phenotype]
MeSH term(s) associated for indexing
- retinal cone photoreceptor cells [MeSH Descriptor]
- retinal degeneration [MeSH Descriptor]
Record concept(s)
- retinal cone dystrophy 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinal cone dystrophy 1 [OMIM Phenotype]

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02/05/2025

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