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717010007: Autosomal dominant Charcot-Marie-Tooth disease type 2C (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
3308175016 Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3308176015 Autosomal dominant Charcot-Marie-Tooth disease type 2C en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5401448014 A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401449018 A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by the association of vocal cord anomalies, impairment of respiratory muscles and sensorineural hearing loss with the distal hands and feet weakness. Onset is between infancy and the 6th decade. 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
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Is a Autosomal dominant hereditary disorder false Inferred relationship Some
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Is a Charcot-Marie-Tooth disease, type II (disorder) false Inferred relationship Some
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Finding site Peripheral nervous system structure true Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Associated morphology Atrophy true Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Finding site Nerve structure true Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder) Is a Autosomal dominant Charcot-Marie-Tooth disease type 2 true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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