cone dystrophy, X-Linked, 1 - CISMeF

" /> cone dystrophy, X-Linked, 1 - CISMeF

CISMeF

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Cone dystrophy, X-Linked, 1MeSH Supplementary Concept

Preferred Label : cone dystrophy, X-Linked, 1;

Details

Origin ID

C564439;

UMLS CUI

C1844777;

Currated CISMeF NLP mapping
- Cone-rod dystrophy, X-linked, 1 [OMIM Phenotype]
- X-linked cone-rod dystrophy 1 [DO Concept]
- cone dystrophy x linked 1 [Disease (Nov.)]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- cone dystrophy, X-Linked, 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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02/05/2025

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