Intellectual Developmental Disorder, Autosomal Dominant 10 (MRD10)

Alias:

Mrd10

Autosomal Dominant Intellectual Developmental Disorder 10

Mental Retardation, Autosomal Dominant 10

Autosomal Dominant Non-Syndromic Intellectual Disability 10

Mental Retardation, Autosomal Dominant, Type 10

Intellectual Disability, Autosomal Dominant 10

Autosomal Dominant Mental Retardation 10

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Intellectual Developmental Disorder, Autosomal Dominant 10, also known as mrd10, is related to gamma heavy chain disease and solitary osseous plasmacytoma. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 10 is CACNG2 (Calcium Voltage-Gated Channel Auxiliary Subunit Gamma 2). Affiliated tissues include brain, and related phenotypes are intellectual disability, moderate and seizure

Related ID：

MALACARDS：INT523

OMIM：614256

MESH：D008607