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58610003: Leber's optic atrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
97397016 Leber's optic atrophy en Synonym Active Entire term case sensitive SNOMED CT core module
797361019 Leber's optic atrophy (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1231857010 Leber hereditary optic neuropathy en Synonym Active Entire term case sensitive SNOMED CT core module
1231858017 LHON - Leber hereditary optic neuropathy en Synonym Active Entire term case sensitive SNOMED CT core module
1231859013 LHON - Leber's hereditary optic neuropathy en Synonym Active Entire term case sensitive SNOMED CT core module
2839596015 Leber optic atrophy en Synonym Active Entire term case sensitive SNOMED CT core module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leber's optic atrophy Is a Congenital anomaly of skeletal muscle false Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Hereditary optic atrophy true Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Disorder of pyruvate metabolism and mitochondrial respiratory chain true Inferred relationship Existential restriction modifier
Leber's optic atrophy Finding site Optic nerve structure false Inferred relationship Existential restriction modifier 1
Leber's optic atrophy Associated morphology Primary atrophy false Inferred relationship Existential restriction modifier 1
Leber's optic atrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Leber's optic atrophy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Degenerative disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Leber's optic atrophy Finding site Optic nerve structure true Inferred relationship Existential restriction modifier 1
Leber's optic atrophy Associated morphology Primary atrophy true Inferred relationship Existential restriction modifier 1
Leber's optic atrophy Is a Maternally inherited mitochondrial deoxyribonucleic acid disease true Inferred relationship Existential restriction modifier
Leber's optic atrophy Is a Inherited metabolic disorder of nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Leber plus disease Is a True Leber's optic atrophy Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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