Parent term(s)
motor neuron disease
+
Term with siblings
amyotrophic lateral sclerosis +
anterior horn cell disease
lateral sclerosis
motor neuritis
+
multisystem proteinopathy
nonparalytic poliomyelitis
progressive bulbar palsy
+
progressive muscular atrophy
scapuloperoneal spinal muscular atrophy
spinal muscular atrophy
+
Child term(s)
amyotrophic lateral sclerosis type 1
amyotrophic lateral sclerosis type 10
amyotrophic lateral sclerosis type 11
amyotrophic lateral sclerosis type 12
amyotrophic lateral sclerosis type 13
amyotrophic lateral sclerosis type 15
amyotrophic lateral sclerosis type 16
amyotrophic lateral sclerosis type 18
amyotrophic lateral sclerosis type 19
amyotrophic lateral sclerosis type 2
amyotrophic lateral sclerosis type 20
amyotrophic lateral sclerosis type 21
amyotrophic lateral sclerosis type 22
amyotrophic lateral sclerosis type 23
amyotrophic lateral sclerosis type 24
amyotrophic lateral sclerosis type 25
amyotrophic lateral sclerosis type 26
amyotrophic lateral sclerosis type 28
amyotrophic lateral sclerosis type 3
amyotrophic lateral sclerosis type 4
amyotrophic lateral sclerosis type 5
amyotrophic lateral sclerosis type 6
amyotrophic lateral sclerosis type 7
amyotrophic lateral sclerosis type 8
amyotrophic lateral sclerosis type 9
frontotemporal dementia and/or amyotrophic lateral sclerosis 1
frontotemporal dementia and/or amyotrophic lateral sclerosis 2
frontotemporal dementia and/or amyotrophic lateral sclerosis 3
frontotemporal dementia and/or amyotrophic lateral sclerosis 4
frontotemporal dementia and/or amyotrophic lateral sclerosis 6
frontotemporal dementia and/or amyotrophic lateral sclerosis 7
juvenile amyotrophic lateral sclerosis type 27
juvenile amyotrophic lateral sclerosis with dementia
sporadic amyotrophic lateral sclerosis
denotes an 'is-a' relationship