Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures, Autosomal Dominant (NDHMSD)

Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures, Autosomal Dominant(来自ICD-11)

别称:

Mental Retardation, Autosomal Dominant 8, Formerly

Ndhmsd

Neurodevelopmental Disorder with Hyperkinetic Movements and with or Without Seizures, Autosomal Dominant

Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures

Intellectual Disability, Autosomal Dominant 8

Mental Retardation, Autosomal Dominant 8

Mrd8, Formerly

Mrd8

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures, Autosomal Dominant, also known as mental retardation, autosomal dominant 8, formerly, is related to neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive and autosomal dominant intellectual developmental disorder 8. An important gene associated with Neurodevelopmental Disorder with or Without Hyperkinetic Movements and Seizures, Autosomal Dominant is GRIN1 (Glutamate Ionotropic Receptor NMDA Type Subunit 1). Affiliated tissues include eye and brain, and related phenotypes are intellectual disability and seizure

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