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


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

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 SNOMED CT core module
3310751019 Autosomal dominant optic atrophy and peripheral neuropathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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