Cataract and microcornea syndrome

disorder

SNOMED 722382006CUI C1861829

Overview

Cataract and microcornea 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.

Decreased corneal diameter

Very frequent (80-99%)HP:0000482

Lens opacities

Very frequent (80-99%)HP:0000518

Near sighted

Frequent (30-79%)HP:0000545

Corneal dystrophy

Occasional (5-29%)HP:0001131

Involuntary, rapid, rhythmic eye movements

Occasional (5-29%)HP:0000639

Iris coloboma

Occasional (5-29%)HP:0000612

Scarring or clouding of the cornea of the eye

Occasional (5-29%)HP:0007957

Related Conditions

Autosomal hereditary disorder(parent)

Microcornea(parent)

Congenital cataract(parent)

Hereditary disorder of the visual system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 722382006
UMLS CUI: C1861829
Fully Specified Name: Cataract and microcornea syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.