progressive myoclonic epilepsy type 3 (Q55345820)

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human disease
  • Epilepsy progressive myoclonic type 3
  • EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS
  • EPM3
  • Progressive myoclonic epilepsy due to KCTD7 deficiency
  • Ceroid Lipofuscinosis, Neuronal, 14
  • EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS; EPM3
  • Progressive myoclonic epilepsy 3
  • EPM 3
  • Progressive myoclonus epilepsy type 3
  • PME type 3
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English
progressive myoclonic epilepsy type 3
human disease
  • Epilepsy progressive myoclonic type 3
  • EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS
  • EPM3
  • Progressive myoclonic epilepsy due to KCTD7 deficiency
  • Ceroid Lipofuscinosis, Neuronal, 14
  • EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS; EPM3
  • Progressive myoclonic epilepsy 3
  • EPM 3
  • Progressive myoclonus epilepsy type 3
  • PME type 3

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