Congenital Horner syndrome

disorder

SNOMED 770626007CUI C1840475

Overview

Congenital Horner syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Congenital Horner syndrome

HP:0006837

Deep set eye

HP:0000490

Heterochromia iridis

HP:0001100

Ipsilateral lack of facial sweating

HP:0007451

Paralysis

HP:0003470

Related Conditions

Autosomal dominant hereditary disorder(parent)

Inherited autonomic nervous system disorder(parent)

Developmental hereditary disorder(parent)

Horner syndrome(parent)

Congenital disease(parent)

Quick Facts

SNOMED CT: 770626007
UMLS CUI: C1840475
Fully Specified Name: Congenital Horner syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 5

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.