usher syndromes

Preferred Label : usher syndromes;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0483844;

UMLS CUI

C0271097;

Automatic exact mappings (from CISMeF team)
- Usher syndrome [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Retinitis pigmentosa-deafness syndrome [OMIM Phenotype]
- Retinitis pigmentosa-deafness syndrome (disorder) [SNOMED CT concept]
- Usher Syndrome [NCIt concept]
- Usher syndrome [PASCAL descriptor]
- Usher syndrome [DO Concept]
- Usher syndrome [Disease (Nov.)]
- Usher syndrome [ICD-11 Subcategory]
- Usher syndrome [ORDO Disease]
- Usher syndrome type 1 (disorder) [SNOMED CT concept]
- Usher's syndrome [MedDRA Preferred Term]
- retinitis pigmentosa-deafness syndrome [SNOMED Notion]
- retinitis pigmentosa-deafness syndrome [DO Concept]
- usher syndrome [MedlinePlus Topic]
MeSH narrower concept(s)
- usher syndrome, type I [MeSH concept]
- usher syndrome, type II [MeSH concept]
- usher syndrome, type III [MeSH concept]
Related record
- usher syndromes [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinitis pigmentosa-deafness syndrome [OMIM Phenotype]
- Retinitis pigmentosa-deafness syndrome (disorder) [SNOMED CT concept]
- Retinitis pigmentosa-deafness-ataxia syndrome (disorder) [SNOMED CT concept]
- Usher Syndrome [NCIt concept]
- Usher syndrome [ORDO Disease]
- Usher syndrome [DO Concept]
- Usher syndrome [Disease (Nov.)]
- Usher's syndrome [MedDRA Preferred Term]
- retinitis pigmentosa-deafness syndrome [SNOMED Notion]
- retinitis pigmentosa-deafness-ataxia syndrome [SNOMED Notion]
- usher syndrome [MedlinePlus Topic]

Keyword's position in hierarchy(ies) :

Main resources

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