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1156823006: Autosomal recessive bilateral optic atrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4578702017 Autosomal recessive bilateral optic atrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4578703010 Autosomal recessive bilateral optic atrophy 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 bilateral optic atrophy Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 1
Autosomal recessive bilateral optic atrophy Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal recessive bilateral optic atrophy Is a Hereditary bilateral optic atrophy true Inferred relationship Existential restriction modifier
Autosomal recessive bilateral optic atrophy Finding site Structure of left optic nerve true Inferred relationship Existential restriction modifier 1
Autosomal recessive bilateral optic atrophy Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 2
Autosomal recessive bilateral optic atrophy Finding site Structure of right optic nerve 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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