Horner syndrome, congenital

Preferred Label : Horner syndrome, congenital;

Type : Phenotype or locus, molecular basis unknown;

Description : Horner syndrome, resulting from unilateral paralysis of the cervical sympathetics, comprises the classic triad of unilateral ptosis, unilateral miosis with anisocoria, and ipsilateral facial anhidrosis. Iris heterochromia may also be present (Takanashi et al., 2003).;

Inheritance : Autosomal dominant;

Prefixed ID : %143000;

Details

Origin ID

143000;

UMLS CUI

C1840475;

Currated CISMeF NLP mapping
- Congenital Horner syndrome [HPO term]
- Congenital Horner syndrome [ORDO Disease]
- Congenital Horner syndrome (disorder) [SNOMED CT concept]
- Congenital Horner's syndrome [MedDRA Preferred Term]
- Horner syndrome, congenital [ICD-11 More detail]
- horner syndrome, congenital [MeSH concept]
- horner syndrome, congenital [MeSH Supplementary Concept]
DO Cross reference
- Horner's syndrome [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Congenital Horner syndrome [HPO term]
- Deeply set eye [HPO term]
- Enophthalmos [HPO term]
- Heterochromia iridis [HPO term]
- Ipsilateral lack of facial sweating [HPO term]
- Paralysis [HPO term]
ORDO concept(s)
- Congenital Horner syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Horner syndrome [HPO term]
- Congenital Horner syndrome [ORDO Disease]
- Congenital Horner syndrome (disorder) [SNOMED CT concept]
- Congenital Horner's syndrome [MedDRA Preferred Term]
- horner syndrome, congenital [MeSH Supplementary Concept]
- horner syndrome, congenital [MeSH concept]

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