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26360005: Hereditary optic atrophy (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
44142012 Hereditary optic atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
756783015 Hereditary optic atrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


30 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary optic atrophy Is a Primary optic atrophy true Inferred relationship Existential restriction modifier
Hereditary optic atrophy Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Hereditary optic atrophy Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
Hereditary optic atrophy Associated morphology Primary atrophy false Inferred relationship Existential restriction modifier 1
Hereditary optic atrophy Finding site Optic nerve structure false Inferred relationship Existential restriction modifier 1
Hereditary optic atrophy Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 1
Hereditary optic atrophy Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 1
Hereditary optic atrophy Is a Inherited optic neuropathy true Inferred relationship Existential restriction modifier
Hereditary optic atrophy Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary motor and sensory neuropathy with optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Dominant hereditary optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Hereditary optic atrophy NOS Is a False Hereditary optic atrophy Inferred relationship Existential restriction modifier
Early-onset X-linked optic atrophy Is a False Hereditary optic atrophy Inferred relationship Existential restriction modifier
Hereditary right optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Hereditary left optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Spastic paraplegia, optic atrophy, neuropathy syndrome Is a False Hereditary optic atrophy Inferred relationship Existential restriction modifier
Wolfram-like syndrome Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Infantile cerebellar and retinal degeneration Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Autosomal recessive optic atrophy type 7 Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Fatal X-linked ataxia with deafness and loss of vision Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Autosomal recessive optic atrophy type 6 Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Childhood-onset autosomal dominant optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
X-linked optic atrophy Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome Is a True Hereditary optic atrophy Inferred relationship Existential restriction modifier
Hereditary optic atrophy NOS Is a False Hereditary optic atrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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