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1197365006: Familial cavitary optic disc anomaly (disorder)


Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4696045016 Familial cavitary optic disc anomaly (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4696046015 Familial CODA (cavitary optic disc anomaly) en Synonym Active Initial character case insensitive SNOMED CT core
4696047012 Familial cavitary optic disc anomaly en Synonym Active Case insensitive SNOMED CT core
4696048019 A rare genetic eye disease with characteristics of congenital profound excavation of the optic nerve head with diminished visual field, in the absence of elevated intraocular pressure. Many patients lack a well-formed retinal artery and have multiple radial cilioretinal arteries instead. The condition is mostly bilateral, may worsen progressively, and is often complicated by serous macular detachment with profound visual loss. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial cavitary optic disc anomaly Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial cavitary optic disc anomaly Is a Optic cupping true Inferred relationship Some
Familial cavitary optic disc anomaly Is a Inherited optic neuropathy true Inferred relationship Some
Familial cavitary optic disc anomaly Is a Developmental hereditary disorder true Inferred relationship Some
Familial cavitary optic disc anomaly Is a Congenital anomaly of optic disc true Inferred relationship Some
Familial cavitary optic disc anomaly Interprets Optic disc cup true Inferred relationship Some 2
Familial cavitary optic disc anomaly Occurrence Congenital true Inferred relationship Some 1
Familial cavitary optic disc anomaly Finding site Optic disc structure true Inferred relationship Some 1
Familial cavitary optic disc anomaly Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Familial cavitary optic disc anomaly Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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