Corneal hypesthesia, familial

Preferred Label : Corneal hypesthesia, familial;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Trigeminal anesthesia, familial;

Inheritance : Autosomal dominant;

Prefixed ID : %122450;

Details

Origin ID

122450;

UMLS CUI

C1852541;

Automatic exact mappings (from CISMeF team)
- Congenital trigeminal anesthesia [ORDO Disease]
Currated CISMeF NLP mapping
- corneal hypesthesia, familial [MeSH concept]
- corneal hypesthesia, familial [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Autosomal dominant inheritance [HPO term]
- Decreased corneal sensation [HPO term]
- Recurrent corneal erosions [HPO term]
ORDO concept(s)
- Congenital trigeminal anesthesia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital trigeminal anaesthesia [MedDRA Preferred Term]
- Congenital trigeminal anesthesia [MedDRA LLT]
- Congenital trigeminal anesthesia (disorder) [SNOMED CT concept]
- corneal hypesthesia, familial [MeSH Supplementary Concept]
- corneal hypesthesia, familial [MeSH concept]

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