Intellectual Developmental Disorder, Autosomal Dominant 39 (MRD39)

Alias:

Mrd39

Myt1l-Related Developmental Delay-Intellectual Disability-Obesity Syndrome

Autosomal Dominant Non-Syndromic Intellectual Disability 39

Autosomal Dominant Intellectual Developmental Disorder 39

Mental Retardation, Autosomal Dominant 39, and Obesity

Mental Retardation, Autosomal Dominant, Type 39

Intellectual Disability, Autosomal Dominant 39

Mental Retardation, Autosomal Dominant 39

Autosomal Dominant Mental Retardation 39

Myt1l-Related Prader-Willi-Like Syndrome

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Intellectual Developmental Disorder, Autosomal Dominant 39, is also known as mrd39. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 39 is MYT1L (Myelin Transcription Factor 1 Like). Affiliated tissues include brain and hypothalamus, and related phenotypes are intellectual disability and global developmental delay

Related ID：

MALACARDS：INT475

OMIM：616521

MESH：D008607