Martinique crinkled retinal pigment epitheliopathy

disorder

SNOMED 1187639002CUI C4310713

Overview

Martinique crinkled retinal pigment epitheliopathy 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.

Choroidal neovascular membrane

Very rare (1-4%)HP:0011506

Decreased visual acuity

HP:0007663

Macular atrophy

HP:0007401

Retinitis pigmentosa

HP:0000510

Related Conditions

Autosomal dominant hereditary disorder(parent)

Pattern dystrophy of macula(parent)

Quick Facts

SNOMED CT: 1187639002
UMLS CUI: C4310713
Fully Specified Name: Martinique crinkled retinal pigment epitheliopathy (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 4

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.