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76976005: Optic atrophy (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
127783019 Optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200625011 Optic nerve atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503423016 OA - Optic atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
817755012 Optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

75 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Optic atrophy Is a Disorder of optic nerve true Inferred relationship Some
Optic atrophy Associated morphology Atrophy false Inferred relationship Some 1
Optic atrophy Finding site Optic nerve structure false Inferred relationship Some 1
Optic atrophy Is a Degenerative disorder false Inferred relationship Some
Optic atrophy Is a Neurological lesion false Inferred relationship Some
Optic atrophy Finding site Optic nerve structure true Inferred relationship Some 1
Optic atrophy Associated morphology Atrophy true Inferred relationship Some 1
Optic atrophy Is a Degenerative disease of the central nervous system true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Optic atrophy secondary to retinal disease Is a True Optic atrophy Inferred relationship Some
Post-compressive optic atrophy Is a False Optic atrophy Inferred relationship Some
Odontotrichomelic syndrome (disorder) Is a False Optic atrophy Inferred relationship Some
Partial optic atrophy Is a True Optic atrophy Inferred relationship Some
Compressive optic atrophy (disorder) Is a True Optic atrophy Inferred relationship Some
Glaucomatous atrophy of optic disc Is a False Optic atrophy Inferred relationship Some
Secondary optic atrophy Is a True Optic atrophy Inferred relationship Some
Complete optic atrophy Is a True Optic atrophy Inferred relationship Some
Optic atrophy associated with retinal dystrophy Is a True Optic atrophy Inferred relationship Some
Primary optic atrophy Is a True Optic atrophy Inferred relationship Some
A rare, genetic, endocrine disorder characterised by type I diabetes mellitus (DM), diabetes insipidus (DI), sensorineural deafness (D), bilateral optical atrophy (OA) and neurological signs. Is a False Optic atrophy Inferred relationship Some
Atrophy of optic disc Is a True Optic atrophy Inferred relationship Some
Retrobulbar optic nerve atrophy Is a True Optic atrophy Inferred relationship Some
Unspecified optic atrophy Is a False Optic atrophy Inferred relationship Some
Optic atrophy NOS Is a False Optic atrophy Inferred relationship Some
Behr syndrome Is a False Optic atrophy Inferred relationship Some
Congenital atrophy of optic nerve (disorder) Is a True Optic atrophy Inferred relationship Some
Optic atrophy of left eye Is a True Optic atrophy Inferred relationship Some
Optic atrophy of right eye Is a True Optic atrophy Inferred relationship Some
Syphilitic optic atrophy (disorder) Is a True Optic atrophy Inferred relationship Some
A rare, genetic, autosomal recessive spastic ataxia disease characterized by onset in early childhood of spastic paraparesis, cerebellar ataxia, dysarthria and optic atrophy. Is a True Optic atrophy Inferred relationship Some
Optic atrophy due to late syphilis (disorder) Is a True Optic atrophy Inferred relationship Some
History of optic atrophy (situation) Associated finding True Optic atrophy Inferred relationship Some 1
A rare mitochondrial disease characterized by signs and symptoms within a phenotypic and metabolic spectrum that includes global developmental delay, hypotonia, intellectual disability, optic atrophy, axonal neuropathy, hypertrophic cardiomyopathy, lactic acidosis, and increased excretion of Krebs cycle intermediates. Other variable features are spasticity, seizures, ataxia, congenital cataract, and dysmorphic facial features. Age of onset is in the neonatal period or infancy. Is a True Optic atrophy Inferred relationship Some
A rare mitochondrial disease characterized by bilateral auditory neuropathy and optic atrophy. Patients present hearing and visual impairment in the first or second decade of life, while psychomotor development is normal. Bilateral retinitis pigmentosa has been reported in association. Is a True Optic atrophy Inferred relationship Some
A rare mitochondrial disease characterized by a variable clinical phenotype with the core features of optic atrophy, ataxia, and hypotonia. Additional common manifestations include global developmental delay with or without regression, neuropathy, spasticity, and microcephaly, less frequently seizures, movement disorder, hearing loss, and respiratory failure. Brain imaging may show abnormalities of the corpus callosum, basal ganglia, and midbrain, cerebral or cerebellar atrophy, or white matter abnormalities. The condition is frequently fatal at an early age. Is a True Optic atrophy Inferred relationship Some

This concept is not in any reference sets

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