63135006: Amyotonia congenita (disorder)

• SNOMED CT Concept\Clinical finding\...
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skeletal muscle\Myoneural disorder\Amyotonia congenita
• \Muscle finding\Myopathy\Disorder of skeletal muscle\Myoneural disorder\Amyotonia congenita
• \Musculoskeletal finding\Musculoskeletal disorder\...
• \Hereditary disorder of musculoskeletal system\Amyotonia congenita
• \Disorder of skeletal muscle\Myoneural disorder\Amyotonia congenita
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Amyotonia congenita
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Amyotonia congenita
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Amyotonia congenita
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Amyotonia congenita
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Amyotonia congenita
• \Disease\Disorder of body system\Neurological disorder\Neuropathy\Neuromuscular junction disorder\Disorder of neuromuscular transmission\Amyotonia congenita
• \Disease\Disorder of body system\Neurological disorder\Hereditary disorder of nervous system\Amyotonia congenita
• \Disease\Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Myoneural disorder\Amyotonia congenita
• \Disease\Disorder of body system\Neurological disorder\Disorder of the peripheral nervous system\Neuromuscular junction disorder\Disorder of neuromuscular transmission\Amyotonia congenita
• \Disease\Disorder of body system\Musculoskeletal disorder\Hereditary disorder of musculoskeletal system\Amyotonia congenita
• \Disease\Disorder of body system\Musculoskeletal disorder\Disorder of skeletal muscle\Myoneural disorder\Amyotonia congenita
• \Disease\Myopathy\Disorder of skeletal muscle\Myoneural disorder\Amyotonia congenita
• \Disease\Congenital disease\Amyotonia congenita
• \Disease\Disorder of soft tissue\Disorder of skeletal muscle\Myoneural disorder\Amyotonia congenita

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
104952014	Amyotonia congenita	en	Synonym	Active	Case insensitive	SNOMED CT core
104953016	Oppenheim's disease	en	Synonym	Active	Case sensitive	SNOMED CT core
104954010	Congenital atonic pseudoparalysis	en	Synonym	Active	Case insensitive	SNOMED CT core
499491010	Oppenheim's amyotonia	en	Synonym	Active	Case sensitive	SNOMED CT core
802385015	Amyotonia congenita (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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