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717975006: Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3310750018 Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310751019 Autosomal dominant optic atrophy and peripheral neuropathy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401659010 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401660017 A rare form of autosomal dominant optic atrophy (ADOA) characterised by progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3310750018 Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310750018 Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310751019 Autosomal dominant optic atrophy and peripheral neuropathy syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3310751019 Autosomal dominant optic atrophy and peripheral neuropathy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3310752014 A form of autosomal dominant optic atrophy with characteristics of progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401659010 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401660017 A rare form of autosomal dominant optic atrophy (ADOA) characterised by progressive and isolated visual loss in the first decade of life, decreased reflexes in the lower limbs and a mild cerebellar stance. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
601291000274118 Autosomal-dominante Optikusatrophie und periphere Neuropathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3449521001000112 Optikusatrophie und periphere Neuropathie, autosomal-dominant de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5805901000241113 syndrome autosomique dominant d'atrophie optique et neuropathie périphérique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5805901000241113 syndrome autosomique dominant d'atrophie optique et neuropathie périphérique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
601291000274118 Autosomal-dominante Optikusatrophie und periphere Neuropathie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3449521001000112 Optikusatrophie und periphere Neuropathie, autosomal-dominant de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) Is a Dominant hereditary optic atrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) Is a Peripheral nerve disease true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) Finding site Peripheral nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder) Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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