Intellectual Developmental Disorder, Autosomal Dominant 3 (MRD3)

Alias:

Mrd3

Autosomal Dominant Intellectual Developmental Disorder 3

Mental Retardation, Autosomal Dominant 3

Autosomal Dominant Non-Syndromic Intellectual Disability 3

Mental Retardation, Autosomal Dominant, Type 3

Intellectual Disability, Autosomal Dominant 3

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Intellectual Developmental Disorder, Autosomal Dominant 3, also known as mrd3, is related to pseudopapilledema and leber congenital amaurosis 15. An important gene associated with Intellectual Developmental Disorder, Autosomal Dominant 3 is CDH15 (Cadherin 15), and among its related pathways/superpathways are Visual phototransduction and Visual Cycle in Retinal Rods. Affiliated tissues include brain and myeloid, and related phenotypes are intellectual disability and seizure

Related ID：

MALACARDS：INT514

OMIM：612580

MESH：D008607