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1156837002: Autosomal dominant distal hereditary motor neuropathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4576298019 Autosomal dominant distal hereditary motor neuropathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4576299010 Autosomal dominant distal hereditary motor neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


8 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant distal hereditary motor neuropathy (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant distal hereditary motor neuropathy (disorder) est un(e) (attribut) Hereditary disorder of nervous system true Inferred relationship Some
Autosomal dominant distal hereditary motor neuropathy (disorder) localisation d'une constatation (attribut) structure d'un nerf true Inferred relationship Some 1
Autosomal dominant distal hereditary motor neuropathy (disorder) localisation d'une constatation (attribut) structure du système nerveux périphérique true Inferred relationship Some 2
Autosomal dominant distal hereditary motor neuropathy (disorder) est un(e) (attribut) Peripheral motor neuropathy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal dominant spastic paraplegia type 17 (disorder) est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
Distal hereditary motor neuropathy type 1 (disorder) est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
Autosomal dominant congenital benign spinal muscular atrophy est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
Distal hereditary motor neuropathy type 5 (disorder) est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some
Distal hereditary motor neuropathy type 2 (disorder) est un(e) (attribut) True Autosomal dominant distal hereditary motor neuropathy (disorder) Inferred relationship Some

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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