715646003: Desmin related myopathy with Mallory body-like inclusions (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Muscle finding (finding)\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\...
• \Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Disease\Disorder of muscle\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle (disorder)\Myopathy with cytoplasmic inclusions (disorder)\Desmin related myopathy with Mallory body-like inclusions (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3303280018	Desmin related myopathy with Mallory body-like inclusions (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303281019	Desmin related myopathy with Mallory body-like inclusions	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303282014	Early onset desmin related myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5401007017	A rare inclusion myopathy characterized by hypotonia and axial muscle weakness leading to spinal rigidity and development of scoliosis and other deformities which can result in respiratory failure. The symptoms are apparent from birth or early childhood. The muscle weakness is not progressive, and most patients remain ambulatory. Muscle biopsies show variable myopathic changes.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401008010	A rare inclusion myopathy characterised by hypotonia and axial muscle weakness leading to spinal rigidity and development of scoliosis and other deformities which can result in respiratory failure. The symptoms are apparent from birth or early childhood. The muscle weakness is not progressive, and most patients remain ambulatory. Muscle biopsies show variable myopathic changes.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3303280018	Desmin related myopathy with Mallory body-like inclusions (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303281019	Desmin related myopathy with Mallory body-like inclusions	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303282014	Early onset desmin related myopathy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303282014	Early onset desmin related myopathy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5401007017	A rare inclusion myopathy characterized by hypotonia and axial muscle weakness leading to spinal rigidity and development of scoliosis and other deformities which can result in respiratory failure. The symptoms are apparent from birth or early childhood. The muscle weakness is not progressive, and most patients remain ambulatory. Muscle biopsies show variable myopathic changes.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401008010	A rare inclusion myopathy characterised by hypotonia and axial muscle weakness leading to spinal rigidity and development of scoliosis and other deformities which can result in respiratory failure. The symptoms are apparent from birth or early childhood. The muscle weakness is not progressive, and most patients remain ambulatory. Muscle biopsies show variable myopathic changes.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3453701001000113	Desmin-abhängige Myopathie mit Mallory Körperchen-ähnlichen Einschlüssen	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
891761000172118	myopathie avec surcharge en desmine et inclusions de corps de Mallory	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
946931000172116	myopathie avec surcharge en desmine de début précoce	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
891761000172118	myopathie avec surcharge en desmine et inclusions de corps de Mallory	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
946931000172116	myopathie avec surcharge en desmine de début précoce	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3453701001000113	Desmin-abhängige Myopathie mit Mallory Körperchen-ähnlichen Einschlüssen	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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