intellectual disability, autosomal dominant 30

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Disease Overview

Any intellectual disability-expressive aphasia-facial dysmorphism syndrome in which the cause of the disease is a mutation in the ZMYND11 gene.

Synonyms

MRD30
ZMYND11 intellectual disability-expressive aphasia-facial dysmorphism syndrome
autosomal dominant intellectual disability 30
autosomal dominant mental retardation 30
autosomal dominant non-syndromic intellectual disability 30
intellectual disability, autosomal dominant 30
intellectual disability, autosomal dominant type 30
intellectual disability-expressive aphasia-facial dysmorphism syndrome caused by mutation in ZMYND11
mental retardation, autosomal dominant 30
mental retardation, autosomal dominant type 30

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.