Also known as:
ALS21, MATR3 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 21, amyotrophic lateral sclerosis caused by mutation in MATR3, amyotrophic lateral sclerosis type 21, myopathy, distal, 2, myopathy, distal, 2, formerly, vocal cord and pharyngeal dysfunction with distal myopathy, vocal cord and pharyngeal dysfunction with distal myopathy, formerly
Also known as:
ALS 22, ALS22, TUBA4A amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 22, amyotrophic lateral sclerosis 22 with or without frontotemporal dementia, amyotrophic lateral sclerosis caused by mutation in TUBA4A, amyotrophic lateral sclerosis type 22
Also known as:
ALS23, amyotrophic lateral sclerosis 23
Also known as:
ALS3, amyotrophic lateral sclerosis 3
Also known as:
ALS 4, ALS4, SETX amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 4, amyotrophic lateral sclerosis 4, juvenile, amyotrophic lateral sclerosis caused by mutation in SETX, dHMN with upper motor neuron signs, distal hereditary motor neuropathy with pyramidal features, distal hereditary motor neuropathy with upper motor neuron signs, neuronopathy, distal hereditary motor, with pyramidal features
Also known as:
ALS5, SPG11 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 5, amyotrophic lateral sclerosis 5, juvenile, amyotrophic lateral sclerosis caused by mutation in SPG11
Also known as:
ALS6, FUS amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 6 with or without frontotemporal dementia, amyotrophic lateral sclerosis 6, with or without frontotemporal dementia, amyotrophic lateral sclerosis caused by mutation in FUS, autosomal recessive amyotrophic lateral sclerosis 6
Also known as:
ALS7, amyotrophic lateral sclerosis 7
Also known as:
ALS8, VAPB amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 8, amyotrophic lateral sclerosis caused by mutation in VAPB, amyotrophic lateral sclerosis type 8
Also known as:
ALS9, ANG amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 9, amyotrophic lateral sclerosis caused by mutation in ANG, amyotrophic lateral sclerosis type 9