Juvenile retinoschisis

disorder

SNOMED 86923008CUI C0271091

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.

Abnormal ERG

Very frequent (80-99%)HP:0000512

Abnormality of vision

Very frequent (80-99%)HP:0000504

Decreased visual acuity, progressive

Very frequent (80-99%)HP:0000529

Eye movement issue

Very frequent (80-99%)HP:0000496

Glaucoma

Very frequent (80-99%)HP:0000501

Retinoschisis

Very frequent (80-99%)HP:0030502

Abnormality of the fovea

Frequent (30-79%)HP:0000493

Electronegative ERG

Frequent (30-79%)HP:0007984

Hyperautofluorescent retinal lesion

Frequent (30-79%)HP:0025158

Retinal pigment epithelial atrophy

Frequent (30-79%)HP:0007722

Vitreous hemorrhage

Frequent (30-79%)HP:0007902

Loss of foveal reflex

Occasional (5-29%)HP:0030825

Mizuo phenomenon

Occasional (5-29%)HP:0030824

Night blindness

Occasional (5-29%)HP:0000662

Retinal detachment

Occasional (5-29%)HP:0000541

Squint

Occasional (5-29%)HP:0000486

Related Conditions

Retinoschisis(parent)

Hereditary retinal dystrophy(parent)

X-linked recessive hereditary disease(parent)

Quick Facts

SNOMED CT: 86923008
UMLS CUI: C0271091
Fully Specified Name: Juvenile retinoschisis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.