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.