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783065004: Autosomal recessive optic atrophy type 7 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3757317014 Autosomal recessive optic atrophy OPA7 type en Synonym Active Only initial character case insensitive SNOMED CT core module
3757318016 Autosomal recessive optic atrophy OPA7 (optic atrophy type 7) en Synonym Active Only initial character case insensitive SNOMED CT core module
3757319012 Autosomal recessive optic atrophy type 7 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3757320018 Autosomal recessive optic atrophy type 7 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 recessive optic atrophy type 7 Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 1
Autosomal recessive optic atrophy type 7 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive optic atrophy type 7 Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive optic atrophy type 7 Is a Hereditary optic atrophy true Inferred relationship Existential restriction modifier
Autosomal recessive optic atrophy type 7 Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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