Amyotrophic lateral sclerosis type 1
Autosomal recessive hereditary disorder
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Autosomal recessive amyotrophic lateral sclerosis type 1 (disorder)
Autosomal recessive amyotrophic lateral sclerosis type 1
ALS1 AR - amyotrophic lateral sclerosis type 1 autosomal recessive
Autosomal recessive ALS (amyotrophic lateral sclerosis) type 1
An autosomal recessive hereditary 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 mutations in the superoxide dismutase-1 gene (SOD1) on chromosome 21q22.
Id1197524007
StatusDefined
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