52647008: Charcot-Marie-Tooth disease, type I (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

198400014 Peroneal muscular atrophy of demyelinating type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

496390011 Hereditary motor and sensory neuropathy type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

496391010 Hereditary sensory and autonomic neuropathy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

496392015 Dominant hereditary sensory neuropathy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

496393013 Acrodystrophic neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

496394019 Charcot-Marie-Tooth disease of demyelinating type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

790679010 Charcot-Marie-Tooth disease, type I (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core

87618018 Charcot-Marie-Tooth disease, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

87619014 Hereditary sensory-motor neuropathy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

87620015 Inherited dominant hypertrophic neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

87621016 HSMN, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Charcot-Marie-Tooth disease, type I (disorder)	est un(e) (attribut)	Neuropathy	false	Inferred relationship	Some
Charcot-Marie-Tooth disease, type I (disorder)	est un(e) (attribut)	Charcot-Marie-Tooth disease (disorder)	false	Inferred relationship	Some
Charcot-Marie-Tooth disease, type I (disorder)	morphologie associée (attribut)	atrophie (anomalie morphologique)	false	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type I (disorder)	morphologie associée (attribut)	Neuropathic atrophy (morphologic abnormality)	false	Inferred relationship	Some	1
Charcot-Marie-Tooth disease, type I (disorder)	localisation d'une constatation (attribut)	structure d'un nerf	false	Inferred relationship	Some
Charcot-Marie-Tooth disease, type I (disorder)	localisation d'une constatation (attribut)	structure du système nerveux périphérique	false	Inferred relationship	Some
Charcot-Marie-Tooth disease, type I (disorder)	localisation d'une constatation (attribut)	structure de muscle squelettique	false	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
maladie de Charcot-Marie-Tooth type 1A (trouble)	est un(e) (attribut)	False	Charcot-Marie-Tooth disease, type I (disorder)	Inferred relationship	Some
maladie de Charcot-Marie-Tooth type 1C (trouble)	est un(e) (attribut)	False	Charcot-Marie-Tooth disease, type I (disorder)	Inferred relationship	Some
maladie de Charcot-Marie-Tooth type 1B (trouble)	est un(e) (attribut)	False	Charcot-Marie-Tooth disease, type I (disorder)	Inferred relationship	Some

Reference Sets

Canada English language reference set (foundation metadata concept)

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)