cataract congenital dominant non nuclear - CISMeF

" /> cataract congenital dominant non nuclear - CISMeF

CISMeF

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Cataract congenital dominant non nuclearMeSH Supplementary Concept

Preferred Label : cataract congenital dominant non nuclear;

MeSH synonym : autosomal dominant nonnuclear polymorphic congenital cataract; cataract, polymorphic congenital; cataract, nonnuclear polymorphic congenital, autosomal dominant;

Details

Origin ID

C538284;

UMLS CUI

C1832526;

CISMeF manual mappings
- obsolete Nonnuclear polymorphic congenital cataract [HPO term]
Currated CISMeF NLP mapping
- Cataract, nonnuclear polymorphic congenital, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
Record concept(s)
- Cataract congenital dominant non nuclear [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cataract, nonnuclear polymorphic congenital, autosomal dominant [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
29/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.

" /> cataract congenital dominant non nuclear - CISMeF

CISMeF

chu

Cataract congenital dominant non nuclearMeSH Supplementary Concept

Preferred Label : cataract congenital dominant non nuclear;

MeSH synonym : autosomal dominant nonnuclear polymorphic congenital cataract; cataract, polymorphic congenital; cataract, nonnuclear polymorphic congenital, autosomal dominant;

Details

Origin ID

C538284;

UMLS CUI

C1832526;

CISMeF manual mappings
- obsolete Nonnuclear polymorphic congenital cataract [HPO term]
Currated CISMeF NLP mapping
- Cataract, nonnuclear polymorphic congenital, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
Record concept(s)
- Cataract congenital dominant non nuclear [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cataract, nonnuclear polymorphic congenital, autosomal dominant [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
29/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.