Familial congenital palsy of trochlear nerve

disorder

SNOMED 782679002CUI C1850996

Overview

Familial congenital palsy of trochlear nerve 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.

Abnormal visual fixation

HP:0025404

Abnormality of binocular vision

HP:0011514

Fourth cranial nerve palsy

HP:0007011

Impaired ocular adduction

HP:0000542

Superior oblique palsy

HP:0025592

Related Conditions

Familial disease(parent)

Congenital trochlear nerve palsy(parent)

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Hereditary disorder of the visual system(parent)

Quick Facts

SNOMED CT: 782679002
UMLS CUI: C1850996
Fully Specified Name: Familial congenital palsy of trochlear nerve (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.