apraxia, oculomotor, cogan type

Preferred Label : apraxia, oculomotor, cogan type;

CISMeF synonym : ocular motor apraxia;

MeSH synonym : congenital oculomotor apraxia; saccade initiation failure, congenital; cogan's syndrome, type 2; oculomotor apraxia, cogan type;

Is substance : O;

Details

Origin ID

C537423;

UMLS CUI

C0543874;

Automatic exact mappings (from CISMeF team)
- Avery's syndrome type 2 (disorder) [SNOMED CT concept]
- Cogan's oculomotor apraxia [MedDRA LLT]
- Duane's syndrome, type 2 (disorder) [SNOMED CT concept]
- Ocular motor apraxia [OMIM Phenotype]
- Oculomotor apraxia [HPO term]
- cogan's syndrome [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital oculomotor apraxia [MedDRA Preferred Term]
- Ocular motor apraxia Cogan type (disorder) [SNOMED CT concept]
- Ocular motor apraxia, Cogan type [ORDO Disease]
HPO term
- Oculomotor apraxia [HPO term]
MeSH term(s) associated for indexing
- apraxias [MeSH Descriptor]
- cogan syndrome [MeSH Descriptor]
ORDO relation(s)
- Ocular motor apraxia, Cogan type [ORDO Disease]
Record concept(s)
- Apraxia, oculomotor, Cogan type [MeSH concept]
- ocular motor apraxia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cogan's oculomotor apraxia [MedDRA LLT]
- Congenital oculomotor apraxia [MedDRA Preferred Term]
- Ocular motor apraxia [OMIM Phenotype]
- Ocular motor apraxia Cogan type (disorder) [SNOMED CT concept]
- Ocular motor apraxia, Cogan type [ORDO Disease]

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