FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

26360005: Hereditary optic atrophy (disorder)


Status: current, 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
44142012 Hereditary optic atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
756783015 Hereditary optic atrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


29 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary optic atrophy est un(e) (attribut) Inherited optic neuropathy true Inferred relationship Some
Hereditary optic atrophy est un(e) (attribut) Hereditary degenerative disease of central nervous system true Inferred relationship Some
Hereditary optic atrophy est un(e) (attribut) Primary optic atrophy true Inferred relationship Some
Hereditary optic atrophy est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some
Hereditary optic atrophy est un(e) (attribut) Hereditary disorder of the visual system false Inferred relationship Some
Hereditary optic atrophy localisation d'une constatation (attribut) Optic nerve structure true Inferred relationship Some 1
Hereditary optic atrophy morphologie associée (attribut) Primary atrophy true Inferred relationship Some 1
Hereditary optic atrophy morphologie associée (attribut) Primary atrophy false Inferred relationship Some 1
Hereditary optic atrophy localisation d'une constatation (attribut) Optic nerve structure false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Infantile cerebellar and retinal degeneration (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Autosomal recessive optic atrophy type 7 (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Arts syndrome est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
SPOAN and SPOAN-related disorder est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Autosomal recessive optic atrophy type 6 est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Childhood-onset autosomal dominant optic atrophy est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
X-linked optic atrophy est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Mitochondrial enoyl coenzyme A reductase protein-associated neurodegeneration syndrome (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Hereditary motor and sensory neuropathy with optic atrophy est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Dominant hereditary optic atrophy est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Leber's optic atrophy (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Hereditary optic atrophy NOS est un(e) (attribut) False Hereditary optic atrophy Inferred relationship Some
Early-onset X-linked optic atrophy (disorder) est un(e) (attribut) False Hereditary optic atrophy Inferred relationship Some
Hereditary right optic atrophy (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Hereditary left optic atrophy (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) est un(e) (attribut) False Hereditary optic atrophy Inferred relationship Some
Wolfram-like syndrome (disorder) est un(e) (attribut) True Hereditary optic atrophy Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

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

GB English

US English

Back to Start