Hyperekplexia 1

MONDO:0007868

A hyperekplexia that has material basis in heterozygous, homozygous, or compound heterozygous mutation in the GLRA1 gene on chromosome 5q32.

Also known as: HKPX1, hyperekplexia 1, hyperekplexia type 1, hyperekplexia, hereditary type 1, Kok disease, Sthe, Stiff-Man syndrome, congenital, Stiff-Person syndrome, congenital

35 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by