prosopagnosia, hereditary - CISMeF

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CISMeF

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Prosopagnosia, hereditaryMeSH Supplementary Concept

Preferred Label : prosopagnosia, hereditary;

MeSH synonym : face blindness; prosopagnosia, congenital;

Details

Origin ID

C537242;

UMLS CUI

C2931455;

Automatic exact mappings (from CISMeF team)
- Blindness [PASCAL descriptor]
- Blindness [NCIt concept]
- Prosopagnosia [NCIt concept]
Currated CISMeF NLP mapping
- Prosopagnosia, hereditary [OMIM Phenotype]
False automatic mappings
- BLINDNESS [WHO-ART Preferred Term]
- Blind [MedDRA LLT]
- Blind (finding) [Inactive SNOMED CT concept]
- Blindness [HPO term]
- Blindness [MedDRA Preferred Term]
- blindness [ICPC-2 Rubric]
- blindness, nos [SNOMED Notion]
- vision impairment and blindness [MedlinePlus Topic]
MeSH term(s) associated for indexing
- prosopagnosia [MeSH Descriptor]
Record concept(s)
- Prosopagnosia, hereditary [MeSH concept]
See also inter- (CISMeF)
- Prosopagnosia [NCIt concept]
- Prosopagnosia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Prosopagnosia, hereditary [OMIM Phenotype]

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25/05/2025

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