Intellectual Developmental Disorder, Autosomal Dominant 41 (MRD41)

Alias:

Mrd41

Autosomal Dominant Intellectual Developmental Disorder 41

Autosomal Dominant Non-Syndromic Intellectual Disability 41

Mental Retardation, Autosomal Dominant, Type 41

Intellectual Disability, Autosomal Dominant 41

Mental Retardation, Autosomal Dominant 41

Autosomal Dominant Mental Retardation 41

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Intellectual Developmental Disorder, Autosomal Dominant 41, also known as mrd41, is related to pierpont syndrome and st. louis encephalitis. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 41 is TBL1XR1 (TBL1X/Y Related 1), and among its related pathways/superpathways are mBDNF and proBDNF regulation of GABA neurotransmission and Rett syndrome causing genes. Affiliated tissues include brain, and related phenotypes are seizure and intellectual disability

Related ID：

MALACARDS：INT550

OMIM：616944

MESH：D008607