Hemifacial hyperplasia strabismus syndrome

disorder

SNOMED 733046006CUI C1841640

Overview

Hemifacial hyperplasia strabismus 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.

Extension of hair growth on temples to lateral eyebrow

Very frequent (80-99%)HP:0005325

Unbalanced face

Very frequent (80-99%)HP:0000324

Increased intercanthal distance

Frequent (30-79%)HP:0000506

Mongoloid slant

Frequent (30-79%)HP:0000582

Open bite

Frequent (30-79%)HP:0010807

Squint

Frequent (30-79%)HP:0000486

Wandering eye

Frequent (30-79%)HP:0000646

Submucous cleft hard palate

Occasional (5-29%)HP:0000176

Friedreich's disease

HP:0005323

Related Conditions

Autosomal dominant hereditary disorder(parent)

Multiple malformation syndrome with facial defects as major feature(parent)

Congenital strabismus(parent)

Hereditary disorder of the visual system(parent)

Hemifacial hyperplasia(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 733046006
UMLS CUI: C1841640
Fully Specified Name: Hemifacial hyperplasia strabismus syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.