RS1064797002 HDAC4
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Associated Conditions
Inborn genetic diseases
Profound intellectual disability
Brachydactyly syndrome type E
Neurodevelopmental disorder with central hypotonia and dysmorphic facies
Chromosome 2q37 deletion syndrome
Inborn genetic diseases
Profound intellectual disability
Brachydactyly syndrome type E
Neurodevelopmental disorder with central hypotonia and dysmorphic facies
Chromosome 2q37 deletion syndrome
Other Variants in HDAC4