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764850002: maladie de Charcot-Marie-Tooth autosomique dominante type 2A2 (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1016271000172114 CMT2A2 - Charcot-Marie-Tooth disease type 2A2 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3655302010 Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3655303017 Autosomal dominant Charcot-Marie-Tooth disease type 2A2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
767231000241116 maladie de Charcot-Marie-Tooth autosomique dominante type 2A2 (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
968091000172111 maladie de Charcot-Marie-Tooth autosomique dominante type 2A2 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3655153016 A subtype of Autosomal dominant Charcot-Marie-Tooth disease type 2 with the childhood onset of distal weakness and areflexia (with earlier and more severe involvement of the lower extremities), reduced sensory modalities (primarily pain and temperature sensation), foot deformities, postural tremor, scoliosis and contractures. Optic atrophy, vocal cord palsy with dysphonia, sensorineural hearing loss, spinal cord abnormalities and hydrocephalus have also been reported. 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 2A2 (disorder) est un(e) (attribut) Autosomal dominant Charcot-Marie-Tooth disease type 2 true Inferred relationship Some
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder false Inferred relationship Some
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) est un(e) (attribut) Charcot-Marie-Tooth disease, type II (disorder) false Inferred relationship Some
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) localisation d'une constatation (attribut) structure du système nerveux périphérique true Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) localisation d'une constatation (attribut) structure d'un nerf true Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) morphologie associée (attribut) atrophie (anomalie morphologique) 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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