Additional Disease Briefs

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

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Rare Disease Database Reports Additional Rare Disease Briefs
amyotrophic lateral sclerosis type 1

Also known as: ALS1, FALS, amyotrophic lateral sclerosis 1, amyotrophic lateral sclerosis 1, autosomal dominant, amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included, amyotrophic lateral sclerosis 1, autosomal recessive, amyotrophic lateral sclerosis 1, familial, amyotrophic lateral sclerosis type 1, amyotrophic lateral sclerosis, autosomal dominant, amyotrophic lateral sclerosis, familial, amyotrophic lateral sclerosis, sporadic, amyotrophic lateral sclerosis, sporadic, included, amyotrophic lateral sclerosis, susceptibility to

amyotrophic lateral sclerosis type 10

Also known as: ALS10, Ftld-TDP, Tardbp-related, TARDBP amyotrophic lateral sclerosis, TARDBP-related frontotemporal lobar degeneration with Tdp43 inclusions, amyotrophic lateral sclerosis 10, amyotrophic lateral sclerosis 10 with or without frontotemporal dementia, amyotrophic lateral sclerosis 10, with or without FTD, amyotrophic lateral sclerosis 10, with or without frontotemporal dementia, amyotrophic lateral sclerosis caused by mutation in TARDBP, amyotrophic lateral sclerosis type 10, frontotemporal dementia with Tdp43 inclusions, Tardbp-related, frontotemporal lobar Degeneration with Tdp43 inclusions, Tardbp-related, frontotemporal lobar degeneration, TARDBP-related

amyotrophic lateral sclerosis type 11

Also known as: ALS11, FIG4 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 11, amyotrophic lateral sclerosis caused by mutation in FIG4, amyotrophic lateral sclerosis type 11

amyotrophic lateral sclerosis type 12

Also known as: ALS12, OPTN amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 12, amyotrophic lateral sclerosis 12 with or without frontotemporal dementia, amyotrophic lateral sclerosis caused by mutation in OPTN, amyotrophic lateral sclerosis type 12

amyotrophic lateral sclerosis type 15

Also known as: ALS15, UBQLN2 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 15, amyotrophic lateral sclerosis 15 with or without frontotemporal dementia, amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant, amyotrophic lateral sclerosis caused by mutation in UBQLN2, amyotrophic lateral sclerosis type 15

amyotrophic lateral sclerosis type 16

Also known as: ALS16, SIGMAR1 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 16, amyotrophic lateral sclerosis 16, juvenile, amyotrophic lateral sclerosis caused by mutation in SIGMAR1

amyotrophic lateral sclerosis type 18

Also known as: ALS18, PFN1 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 18, amyotrophic lateral sclerosis caused by mutation in PFN1, amyotrophic lateral sclerosis type 18

amyotrophic lateral sclerosis type 19

Also known as: ALS19, ERBB4 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 19, amyotrophic lateral sclerosis caused by mutation in ERBB4, amyotrophic lateral sclerosis type 19

amyotrophic lateral sclerosis type 2, juvenile

Also known as: ALS, juvenile, ALS2, ALS2 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 2, amyotrophic lateral sclerosis 2, juvenile, amyotrophic lateral sclerosis caused by mutation in ALS2

amyotrophic lateral sclerosis type 20

Also known as: ALS20, HNRNPA1 amyotrophic lateral sclerosis, amyotrophic lateral sclerosis 20, amyotrophic lateral sclerosis caused by mutation in HNRNPA1, amyotrophic lateral sclerosis type 20

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