FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

58610003: opticusatrofie van Leber (aandoening)


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
97397016 Leber's 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
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
59061000146117 opticusatrofie van Leber nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
937021000146112 opticusatrofie van Leber (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
1857981000146116 LOA nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


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 Some
Leber's optic atrophy Is a Mitochondrial cytopathy (disorder) true Inferred relationship Some
Leber's optic atrophy Is a Hereditary optic atrophy true Inferred relationship Some
Leber's optic atrophy Is a Congenital anomaly of head false Inferred relationship Some
Leber's optic atrophy Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Leber's optic atrophy Is a Disorder of pyruvate metabolism and mitochondrial respiratory chain true Inferred relationship Some
Leber's optic atrophy Finding site Optic nerve structure false Inferred relationship Some 1
Leber's optic atrophy Associated morphology Primary atrophy false Inferred relationship Some 1
Leber's optic atrophy Occurrence Congenital true Inferred relationship Some 2
Leber's optic atrophy Finding site Skeletal muscle structure false Inferred relationship Some
Leber's optic atrophy Is a Degenerative disorder of musculoskeletal system false Inferred relationship Some
Leber's optic atrophy Finding site Optic nerve structure true Inferred relationship Some 1
Leber's optic atrophy Associated morphology Primary atrophy true Inferred relationship Some 1
Leber's optic atrophy Is a Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder) true Inferred relationship Some
Leber's optic atrophy Is a Inherited metabolic disorder of nervous system true Inferred relationship Some
Leber's optic atrophy Is a Congenital neurological disorder (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Leber plus disease (disorder) Is a True Leber's optic atrophy Inferred relationship Some

Reference Sets

Dutch pathology simple reference set (foundation metadata concept)

Back to Start