Intellectual Developmental Disorder, Autosomal Dominant 2 (MRD2)

Alias:

Mrd2

Autosomal Dominant Intellectual Developmental Disorder 2

Autosomal Dominant Non-Syndromic Intellectual Disability 2

Mental Retardation, Autosomal Dominant, Type 2

Intellectual Disability, Autosomal Dominant 2

Mental Retardation, Autosomal Dominant 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Intellectual Developmental Disorder, Autosomal Dominant 2, also known as mrd2, is related to immunodeficiency 40 and ritscher-schinzel syndrome. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 2 is MRD2 (Mental Retardation, Autosomal Dominant 2). Affiliated tissues include eye and thyroid, and related phenotypes are intellectual disability and global developmental delay

Related ID：

MALACARDS：INT521

OMIM：614113

MESH：D008607