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715799004: Charcot-Marie-Tooth disease type 4G (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303751011 Charcot-Marie-Tooth disease type 4G (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303752016 Charcot-Marie-Tooth disease type 4G en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303753014 Hereditary motor and sensory neuropathy Russe type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5401104010 Charcot-Marie-Tooth disease type 4G (CMT4G) is a subtype of Charcot-Marie-Tooth disease type 4 characterized by early childhood onset of progressive distal muscle weakness and atrophy, delayed motor development, prominent distal sensory impairment, areflexia, moderately reduced nerve conduction velocities, and foot and hand deformities in Balkan (Russe) Gypsies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401105011 Charcot-Marie-Tooth disease type 4G (CMT4G) is a subtype of Charcot-Marie-Tooth disease type 4 characterised by early childhood onset of progressive distal muscle weakness and atrophy, delayed motor development, prominent distal sensory impairment, areflexia, moderately reduced nerve conduction velocities, and foot and hand deformities in Balkan (Russe) Gypsies. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Charcot-Marie-Tooth disease type 4G (disorder) Is a Charcot-Marie-Tooth disease type 4 (disorder) true Inferred relationship Some
Charcot-Marie-Tooth disease type 4G (disorder) Finding site Peripheral nervous system structure false Inferred relationship Some
Charcot-Marie-Tooth disease type 4G (disorder) Occurrence Congenital true Inferred relationship Some 1
Charcot-Marie-Tooth disease type 4G (disorder) Finding site Peripheral nervous system structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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