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838345001: Autosomal recessive optic atrophy type 6 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3896534015 Autosomal recessive optic atrophy type 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3896535019 Autosomal recessive optic atrophy type 6 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3896534015 Autosomal recessive optic atrophy type 6 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3896535019 Autosomal recessive optic atrophy type 6 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
508431000274117 OPA6 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
589731000274119 Autosomal-rezessive Optikusatrophie, Typ 6 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5751121000241111 atrophie optique autosomique récessive de type 6 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5751121000241111 atrophie optique autosomique récessive de type 6 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
508431000274117 OPA6 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
589731000274119 Autosomal-rezessive Optikusatrophie, Typ 6 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 recessive optic atrophy type 6 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive optic atrophy type 6 (disorder) Is a Hereditary optic atrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive optic atrophy type 6 (disorder) Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive optic atrophy type 6 (disorder) Finding site Optic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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