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

Interested in exploring the database in detail?
Click here to explore the database in alphabetical order.

NORD Summit 2026 Banner Ad
Rare Disease Database Reports Additional Rare Disease Briefs
epilepsy, familial adult myoclonic, 1

Also known as: FAME1, benign adult familial myoclonic epilepsy 1, cortical myoclonic tremor with epilepsy, familial, 1, epilepsy, familial ADULT myoclonic, 1

epilepsy, familial adult myoclonic, 2

Also known as: ADRA2B epilepsy, familial adult myoclonic, FAME2, benign adult familial myoclonic epilepsy 2, cortical myoclonic tremor with epilepsy, familial, 2, cortical myoclonus and epilepsy, autosomal dominant, epilepsy, familial ADULT myoclonic, 2, epilepsy, familial adult myoclonic caused by mutation in ADRA2B, epilepsy, familial adult myoclonic, 2, epilepsy, familial adult myoclonic, type 2

epilepsy, familial adult myoclonic, 5

Also known as: CNTN2 epilepsy, familial adult myoclonic, FAME5, cortical myoclonic tremor with epilepsy, familial, 5, epilepsy, familial ADULT myoclonic, 5, epilepsy, familial adult myoclonic caused by mutation in CNTN2, epilepsy, familial adult myoclonic, 5, epilepsy, familial adult myoclonic, type 5, epilepsy, myoclonic, familial adult, 5

epilepsy, familial adult myoclonic, 6

Also known as: FAME6, benign Adult Familial myoclonic epilepsy 6, cortical myoclonic tremor with epilepsy, Familial, 6, epilepsy, FAMILIAL ADULT myoclonic, 6

epilepsy, familial adult myoclonic, 7

Also known as: FAME7, benign Adult Familial myoclonic epilepsy 7, cortical myoclonic tremor with epilepsy, Familial, 7, epilepsy, FAMILIAL ADULT myoclonic, 7

  2. 1
  3. ...
  4. 360
  5. 361
  6. 362
  7. 363
  8. 364
  9. 365
  10. 366
  11. ...
  12. 1032