Pigment dispersion syndrome

disorder

SNOMED 392133001CUI C1271398

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Near sighted

HP:0000545

Optic atrophy

HP:0000648

Primary open angle glaucoma

HP:0012108

Related Conditions

Pigment dispersion syndrome of right eye(child)

Pigment dispersion syndrome of left eye(child)

Iris lesion(parent)

Disorder of pigmentation(parent)

Quick Facts

SNOMED CT: 392133001
UMLS CUI: C1271398
Fully Specified Name: Pigment dispersion syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 3

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.