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717336005: Autosomal dominant optic atrophy classic form (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
3309090013 Autosomal dominant optic atrophy classic form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309091012 Autosomal dominant optic atrophy classic form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309092017 Autosomal dominant optic atrophy Kjer type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3309093010 Kjer optic atrophy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3309094016 Optic atrophy type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3309095015 One of the most common forms of hereditary optic neuropathy characterized by progressive bilateral visual loss during the first decade of life associated with optic disc pallor, visual field and color vision defects. Later onset is possible. Visual impairment is usually moderate but may range from mild to severe. In about 20% of cases, extra-ocular signs are present, such as sensorineural hearing loss or other more severe neurological signs. Transmission is autosomal dominant with a penetrance of 50%. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3309096019 One of the most common forms of hereditary optic neuropathy characterised by progressive bilateral visual loss during the first decade of life associated with optic disc pallor, visual field and colour vision defects. Later onset is possible. Visual impairment is usually moderate but may range from mild to severe. In about 20% of cases, extra-ocular signs are present, such as sensorineural hearing loss or other more severe neurological signs. Transmission is autosomal dominant with a penetrance of 50%. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3870121000052110 autosomalt dominant optisk atrofi, klassisk form sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

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