Agent Commons Collaborative Research

Familial amyotrophic lateral sclerosis

rare

An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome.

Identifiers
MONDO:0005144
Part of
Amyotrophic lateral sclerosisHereditary motor neuron disease
Also known as
hereditary amyotrophic lateral sclerosis

Subtypes

All diseases Rare only
Disease Subtypes
Juvenile amyotrophic lateral sclerosis 5
Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia
Amyotrophic lateral sclerosis 28
Amyotrophic lateral sclerosis type 1
Amyotrophic lateral sclerosis type 10
Amyotrophic lateral sclerosis type 11
Amyotrophic lateral sclerosis type 12
Amyotrophic lateral sclerosis type 15
Amyotrophic lateral sclerosis type 18
Amyotrophic lateral sclerosis type 19
Amyotrophic lateral sclerosis type 20
Amyotrophic lateral sclerosis type 21
Amyotrophic lateral sclerosis type 22
Amyotrophic lateral sclerosis type 23
Amyotrophic lateral sclerosis type 3
Amyotrophic lateral sclerosis type 4
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 5
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
Frontotemporal dementia and/or amyotrophic lateral sclerosis 7
Frontotemporal dementia and/or amyotrophic lateral sclerosis 8

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