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715374003: Autosomal dominant optic atrophy plus syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302395011 Autosomal dominant optic atrophy plus syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3302396012 Autosomal dominant optic atrophy plus syndrome en Synonym Active Case insensitive SNOMED CT core
5048275014 ADOA (autosomal dominant optic atrophy) plus en Synonym Active Case sensitive SNOMED CT core
3302397015 A variant of autosomal dominant optic atrophy associating 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, multiple-sclerosis like illness. ADOA plus is caused by mutations in the OPA1 gene (3q29), encoding a dynamin-like GTPase involved in the fusion of the inner mitochondrial membrane. The phenotypes observed in ADOA plus are thus related to mitochondrial DNA instability resulting in multiple mitochondrial DNA deletions. Transmission is autosomal dominant with variable penetrance. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant optic atrophy plus syndrome Is a Dominant hereditary optic atrophy true Inferred relationship Some
Autosomal dominant optic atrophy plus syndrome Is a Mitochondrial cytopathy true Inferred relationship Some
Autosomal dominant optic atrophy plus syndrome Associated morphology Primary atrophy true Inferred relationship Some 1
Autosomal dominant optic atrophy plus syndrome Finding site Optic nerve structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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