770786001: myopathie à corps d'inclusion héréditaire type 4 (trouble)

• SNOMED CT Concept\constatation clinique\...
• \constatation générale à propos des tissus mous\Disorder of soft tissue\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \constatation à propos d'un muscle\affection musculaire\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Musculoskeletal finding\maladie du système musculosquelettique (trouble)\...
• \Hereditary disorder of musculoskeletal system\myopathie à corps d'inclusion héréditaire type 4
• \affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\myopathie à corps d'inclusion héréditaire type 4
• \Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\myopathie à corps d'inclusion héréditaire type 4
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\myopathie à corps d'inclusion héréditaire type 4
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\myopathie à corps d'inclusion héréditaire type 4
• \Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Hereditary disorder of musculoskeletal system\myopathie à corps d'inclusion héréditaire type 4
• \Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Disease\affection d'un système corporel\maladie du système musculosquelettique (trouble)\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Disease\affection musculaire\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Disease\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Disease\Disorder of soft tissue\affection d'un muscle squelettique\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4
• \Disease\trouble du développement\Developmental hereditary disorder\myopathie à corps d'inclusion héréditaire type 4
• \Disease\trouble du développement\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Myopathy with cytoplasmic inclusions\myopathie à corps d'inclusion héréditaire type 4

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
1015471000172118	myopathie à corps d'inclusion héréditaire type 4	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
1017291000172112	HIBM4 - hereditary inclusion body myopathy type 4	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3702791012	Hereditary inclusion body myopathy type 4 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3702792017	Hereditary inclusion body myopathy type 4	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
769901000241114	myopathie à corps d'inclusion héréditaire type 4 (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3702793010	A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usually preserved. Congophilic inclusions with cytoplasmic inclusions of 15-21 nm filaments on electron microscopy are revealed in muscle biopsy.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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