Hyperekplexia 3
MONDO:0013827Any hereditary hyperekplexia in which the cause of the disease is a mutation in the SLC6A5 gene.
Also known as: HKPX3, SLC6A5 hereditary hyperekplexia, hereditary hyperekplexia caused by mutation in SLC6A5, hyperekplexia 3, hyperekplexia type 3
12 clinical trials for this condition and its sub-types, 0 tagged with Hyperekplexia 3 itself.
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