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Code System Concept

Code System Concept Code	305719002
Code System Concept Name	Neuromyotonia (disorder)
Code System Preferred Concept Name	Neuromyotonia (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Active
SDO Concept Status Date	01/31/2002
SDO Date Created	01/31/2002
SDO Date Revised	01/31/2002
Description
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
448235011	Neuromyotonia	Active	Synonym	false	false
448236012	Continuous muscle fiber activity	Active	Synonym	false	false
448237015	Gamstorp-Wohlfart syndrome	Active	Synonym	false	false
448238013	Gamstorp disease	Active	Synonym	false	false
448239017	Continuous muscle fibre activity	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Birth Defect Diagnosis	1
Clinical Finding (NNDSS)	2 , 1
Disease	10 , 9 , 8 , 7 , 6 , 5 , 4 , 3 , 2 , 1
Problem Value Set	3 , 2

Parent Concepts Parent Concepts Parent/Child (Relationship Type) Disorders of spinal neurones manifest by hyperactivity (disorder) {230651008 , SNOMED-CT } Motor neuron disease (disorder) {37340000 , SNOMED-CT } Peripheral nerve disease (disorder) {302226006 , SNOMED-CT }	Other Relationships No other relationships present.
Child Concepts Neuromyotonia (disorder) {305719002 , SNOMED-CT } Parent/Child (Relationship Type) Autosomal recessive axonal neuropathy with neuromyotonia (disorder) {711406009 , SNOMED-CT }