Amyotrophic lateral sclerosis
Autosomal dominant hereditary disorder
Chronic nervous system disorder
Degenerative disorder
Hereditary disorder of nervous system
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Amyotrophic lateral sclerosis type 3 (disorder)
Amyotrophic lateral sclerosis type 3
ALS3 - amyotrophic lateral sclerosis type 3
A neurodegenerative disease with characteristics of progressive muscular paralysis reflecting degeneration of motor neurons in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. Associated with the ALS3 gene on the cytogenetic location 18q21.
Id1201950008
StatusPrimitive
Clinical courseProgressive
Associated morphologyDegenerative abnormality
Finding siteStructure of nervous system
ICD-10 complex map reference set
TargetG12.2
RuleTRUE
AdviceALWAYS G12.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified