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1187617004: Charcot-Marie-Tooth disease type 2S (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4674375012 Charcot-Marie-Tooth disease type 2S en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674376013 Charcot-Marie-Tooth disease type 2S (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4674377016 A rare subtype of axonal hereditary motor and sensory neuropathy with characteristics of progressive distal muscle weakness and atrophy of both the lower and upper limbs, absent or reduced deep tendon reflexes, mild sensory loss, foot drop and pes cavus leading eventually to wheelchair dependance. Some patients present with early hypotonia and delayed motor development. Scoliosis and variable autonomic disturbances may be associated. 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 2S Is a Autosomal recessive Charcot-Marie-Tooth disease type 2 true Inferred relationship Some
Charcot-Marie-Tooth disease type 2S Finding site Peripheral nervous system structure true Inferred relationship Some 2
Charcot-Marie-Tooth disease type 2S Finding site Nerve structure true Inferred relationship Some 1
Charcot-Marie-Tooth disease type 2S Associated morphology Atrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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