FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

398040009: neuropathie sensitivomotrice héréditaire de type I (trouble)


Status: current, 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
1765959019 Charcot-Marie-Tooth disease, type I (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1777611019 Charcot-Marie-Tooth disease, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786062015 Hereditary sensory-motor neuropathy, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786063013 Peroneal muscular atrophy of demyelinating type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786064019 Inherited dominant hypertrophic neuropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786065018 Hereditary motor and sensory neuropathy type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786066017 Charcot-Marie-Tooth disease of demyelinating type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786067014 HSMN, type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2966574017 Charcot Marie Tooth disease, type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3386401010 neuropathie sensitivo-motrice héréditaire de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
368251000172118 neuropathie sensitivomotrice héréditaire type 1 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
617961000172116 neuropathie sensitivomotrice héréditaire de type I fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
629201000241118 neuropathie sensitivomotrice héréditaire de type I (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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) localisation d'une constatation (attribut) structure du système nerveux périphérique true 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 de muscle squelettique false Inferred relationship Some 1
Charcot-Marie-Tooth disease, type I (disorder) localisation d'une constatation (attribut) structure de muscle squelettique 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) est un(e) (attribut) Hereditary motor and sensory neuropathy (disorder) true Inferred relationship Some
Charcot-Marie-Tooth disease, type I (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
PMP2-related Charcot-Marie-Tooth disease type 1 est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some
maladie de Charcot-Marie-Tooth type 1A (trouble) est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some
maladie de Charcot-Marie-Tooth type 1C (trouble) est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some
maladie de Charcot-Marie-Tooth type 1B (trouble) est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some
Charcot-Marie-Tooth disease type IE (disorder) est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some
maladie de Charcot-Marie-Tooth type 1D est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some
Charcot-Marie-Tooth disease type IF (disorder) est un(e) (attribut) True Charcot-Marie-Tooth disease, type I (disorder) Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start