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58610003: Leber's optic atrophy (disorder)


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

Descriptions:

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


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leber's optic atrophy (disorder) est un(e) (attribut) Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) true Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Inherited metabolic disorder of nervous system true Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) affection dégénérative du système musculosquelettique false Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Congenital anomaly of skeletal muscle false Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Mitochondrial cytopathy true Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Hereditary optic atrophy true Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Congenital anomaly of head false Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Hereditary disorder of musculoskeletal system false Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) Disorder of pyruvate metabolism and mitochondrial respiratory chain true Inferred relationship Some
Leber's optic atrophy (disorder) localisation d'une constatation (attribut) Optic nerve structure true Inferred relationship Some 1
Leber's optic atrophy (disorder) morphologie associée (attribut) Primary atrophy true Inferred relationship Some 1
Leber's optic atrophy (disorder) localisation d'une constatation (attribut) Optic nerve structure false Inferred relationship Some 1
Leber's optic atrophy (disorder) morphologie associée (attribut) Primary atrophy false Inferred relationship Some 1
Leber's optic atrophy (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Leber's optic atrophy (disorder) localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Leber plus disease (disorder) est un(e) (attribut) True Leber's optic atrophy (disorder) Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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