Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome

disorder

SNOMED 773690008CUI C4751163

Overview

Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma 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.

Coloboma of choroid

Very frequent (80-99%)HP:0000567

Decreased corneal diameter

Very frequent (80-99%)HP:0000482

Persistent hyperplasia of primary vitreous

Very frequent (80-99%)HP:0007968

Posterior lenticonus

Very frequent (80-99%)HP:0011502

Breakdown of light-sensitive cells in back of eye

Frequent (30-79%)HP:0000556

Iris coloboma

Frequent (30-79%)HP:0000612

Abnormally small eyeball

Occasional (5-29%)HP:0000568

Related Conditions

Fundus coloboma(parent)

Microcornea(parent)

Posterior lenticonus(parent)

Quick Facts

SNOMED CT: 773690008
UMLS CUI: C4751163
Fully Specified Name: Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma 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.