G12.0 |
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
|
G12.1 |
Other inherited spinal muscular atrophy
Progressive bulbar palsy of childhood [Fazio-Londe]
Spinal muscular atrophy:
adult form
childhood form, type II
distal
juvenile form, type III [Kugelberg-Welander]
scapuloperoneal form
|
G12.2 |
Motor neuron disease
Familial motor neuron disease
Lateral sclerosis:
amyotrophic
primary
Progressive:
bulbar palsy
spinal muscular atrophy
|
G12.8 |
Other spinal muscular atrophies and related syndromes
|
G12.9 |
Spinal muscular atrophy, unspecified
|