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2065009: Dominant hereditary optic atrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4555010 Dominant hereditary optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
749857010 Dominant hereditary optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1222464011 Autosomal dominant optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4394051000241116 atrophie optique héréditaire dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
649981000274118 ADOA de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
649991000274116 Autosomal-dominante Optikusatrophie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dominant hereditary optic atrophy Is a Autosomal dominant hereditary disorder (disorder) true Inferred relationship Some
Dominant hereditary optic atrophy Is a Hereditary optic atrophy true Inferred relationship Some
Dominant hereditary optic atrophy Finding site Optic nerve structure false Inferred relationship Some 1
Dominant hereditary optic atrophy Associated morphology Primary atrophy (morphologic abnormality) false Inferred relationship Some 1
Dominant hereditary optic atrophy Is a Inherited optic neuropathy false Inferred relationship Some
Dominant hereditary optic atrophy Finding site Optic nerve structure true Inferred relationship Some 1
Dominant hereditary optic atrophy Associated morphology Primary atrophy (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare neuro-ophthalmological disease associating the typical optic atrophy with other extra-ocular manifestations such as sensorineural deafness, myopathy, chronic progressive external ophthalmoplegia, ataxia and peripheral neuropathy. More rarely, other manifestations have been associated with this condition, such as spastic paraplegia or multiple-sclerosis like illness. Is a True Dominant hereditary optic atrophy Inferred relationship Some
A rare neuro-ophthalmological disease which is one of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss with an onset during the first decade of life, associated with optic disc pallor, visual acuity loss, visual field deficits and color vision defects. Is a True Dominant hereditary optic atrophy Inferred relationship Some
A rare form of autosomal dominant optic atrophy (ADOA) characterized by progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance. Is a True Dominant hereditary optic atrophy Inferred relationship Some
A form of autosomal dominant optic atrophy characterized by an early and bilateral optic atrophy leading to insidious visual loss of variable severity, followed by a late anterior and/or posterior cortical cataract. Additional features include sensorineural hearing loss and neurological signs such as tremor, extrapyramidal rigidity and absence of deep tendon reflexes. It is caused by mutations in the OPA3 gene (19q13.32). Is a True Dominant hereditary optic atrophy Inferred relationship Some
Optic atrophy-intellectual disability syndrome is a rare, hereditary, syndromic intellectual disability characterized by developmental delay, intellectual disability, and significant visual impairment due to optic nerve atrophy, optic nerve hypoplasia or cerebral visual impairment. Other common clinical signs and symptoms are hypotonia, oromotor dysfunction, seizures, autism spectrum disorder, and repetitive behaviors. Dysmorphic facial features are variable and nonspecific. Is a True Dominant hereditary optic atrophy Inferred relationship Some

Reference Sets

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