6.1.c

Glutamate neurotransmitter disorders

  • Ionotropic glutamate receptor NMDA type subunit 1 dysregulation Autosomal dominant intellectual disability type 8; neurodevelopmental disorder with or without hyperkinetic movements and seizures
  • Ionotropic glutamate receptor NMDA type subunit 2A dysregulation
  • Ionotropic glutamate receptor NMDA type subunit 2B dysregulation (Early infantile epileptic encephalopathy type 27; autosomal dominant intellectual disability type 6)
  • Ionotropic glutamate receptor NMDA type subunit 2D superactivity (Early infantile epileptic encephalopathy type 46)
  • Ionotropic glutamate receptor AMPA type subunit 2 deficiency
  • Ionotropic glutamate receptor AMPA type subunit 3 deficiency (Syndromic X-linked intellectual disability, Wu type)
  • Ionotropic glutamate receptor AMPA type subunit 4 dysregulation (Neurodevelopmental disorder with or without seizures and gait abnormalities – NEDSGA)
  • Ionotropic glutamate receptor delta type subunit 2 deficiency (Autosomal recessive spinocerebellar ataxia type 18)
  • Thorase deficiency (Hyperekplexia type 4)
  • Metabotropic glutamate receptor 1 deficiency (Autosomal recessive spinocerebellar ataxia type 13)
  • Metabotropic glutamate receptor 1 superactivity (Autosomal recessive spinocerebellar ataxia type 44)
  • Metabotropic glutamate receptor 6 deficiency (Congenital stationary night blindness type 1B)

Subnetworks

Immagini SNW 344 x 258 px 1

NOMS

Disorders of neuromodulators and other small molecules

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