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771081007: neuropathie motrice distale héréditaire type 7 (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1001821000172118 atrophie musculaire spinale distale avec paralysie des cordes vocales fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
1002071000172115 neuropathie motrice distale héréditaire type 7 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3704240014 Distal hereditary motor neuropathy type 7 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3704241013 Distal spinal muscular atrophy with vocal cord paralysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3704242018 Distal hereditary motor neuropathy type 7 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
770161000241113 neuropathie motrice distale héréditaire type 7 (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3704245016 A rare slowly progressive genetic peripheral neuropathy with characteristics of distal atrophy and weakness affecting the upper limbs (with a predilection for the thenar eminence) and subsequently the lower limbs, associated with unilateral or bilateral vocal cord paresis leading to hoarse voice, breathing difficulties and facial weakness. 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
neuropathie motrice distale héréditaire type 7 interprète (attribut) Movement (observable entity) true Inferred relationship Some 5
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) Nerve palsy true Inferred relationship Some
neuropathie motrice distale héréditaire type 7 localisation d'une constatation (attribut) structure du système nerveux périphérique true Inferred relationship Some 3
neuropathie motrice distale héréditaire type 7 localisation d'une constatation (attribut) structure d'un nerf true Inferred relationship Some 6
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) Autosomal dominant distal hereditary motor neuropathy (disorder) true Inferred relationship Some
neuropathie motrice distale héréditaire type 7 interprète (attribut) mobilité globale du tronc et des membres true Inferred relationship Some 1
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) trouble neurologique chronique true Inferred relationship Some
neuropathie motrice distale héréditaire type 7 localisation d'une constatation (attribut) Vocal cord structure true Inferred relationship Some 4
neuropathie motrice distale héréditaire type 7 a pour interprétation (attribut) Absent true Inferred relationship Some 1
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) Vocal cord paralysis true Inferred relationship Some
neuropathie motrice distale héréditaire type 7 évolution clinique (attribut) progressif true Inferred relationship Some 2
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) Autosomal dominant hereditary disorder false Inferred relationship Some
neuropathie motrice distale héréditaire type 7 localisation d'une constatation (attribut) système nerveux false Inferred relationship Some 3
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) Chronic disease of respiratory system true Inferred relationship Some
neuropathie motrice distale héréditaire type 7 est un(e) (attribut) Distal spinal muscular atrophy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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