Familial CODA (cavitary optic disc anomaly)

disorder

SNOMED 1197365006CUI C1969063

Overview

Familial CODA (cavitary optic disc anomaly) 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.

Difficulties with night vision

Occasional (5-29%)HP:0000662

Peripapillary atrophy

Very rare (1-4%)HP:0500087

Decreased visual acuity

HP:0007663

Partial loss of field of vision

HP:0001123

Related Conditions

Autosomal dominant hereditary disorder(parent)

Inherited optic neuropathy(parent)

Developmental hereditary disorder(parent)

Congenital anomaly of optic disc(parent)

Quick Facts

SNOMED CT: 1197365006
UMLS CUI: C1969063
Fully Specified Name: Familial cavitary optic disc anomaly (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.

Familial CODA (cavitary optic disc anomaly) — Symptoms, Testing & Specialists | Ltrl