1201861004: Autosomal dominant central core disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Musculoskeletal finding\Musculoskeletal disorder\...
• \Hereditary disorder of musculoskeletal system\Central core disease\Autosomal dominant central core disease
• \Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Central core disease\Autosomal dominant central core disease
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Central core disease\Autosomal dominant central core disease
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Central core disease\Autosomal dominant central core disease
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant central core disease
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Central core disease\Autosomal dominant central core disease
• \Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Central core disease\Autosomal dominant central core disease
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Disease\Disorder of body system\Musculoskeletal disorder\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Disease\Myopathy\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease
• \Disease\Developmental disorder\Developmental hereditary disorder\Central core disease\Autosomal dominant central core disease
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of musculoskeletal system\Congenital anomaly of muscle AND/OR tendon\Congenital anomaly of skeletal muscle\Central core disease\Autosomal dominant central core disease

Status: current, Defined. Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4945365014	Autosomal dominant central core disease (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4945366010	Autosomal dominant central core disease	en	Synonym	Active	Case insensitive	SNOMED CT core
4945367018	Autosomal dominant central core myopathy	en	Synonym	Active	Case insensitive	SNOMED CT core
4945368011	An autosomal dominant hereditary neuromuscular disorder with characteristics of central cores on muscle biopsy and clinical features of a congenital myopathy. Typical presentation is in infancy with hypotonia and motor developmental delay and predominantly proximal weakness pronounced in the hip girdle. Caused by mutations in the skeletal muscle ryanodine receptor (RYR1) gene, encoding the principal skeletal muscle sarcoplasmic reticulum calcium release channel (RyR1). Altered excitability and/or changes in calcium homeostasis within muscle cells due to mutation-induced conformational changes in the RyR protein are considered to be the main pathogenetic mechanism(s).	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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