Elejalde syndrome (also known as "Griscelli syndrome type 1") is a rare autosomal recessive syndrome consisting of moderate pigment dilution, profound primary neurologic defects, no immune defects, and hair with metallic silvery sheen.:866
It is associated with MYO5A.
M: INT, SF, LCT
noco (i/b/d/q/u/r/p/m/k/v/f)/cong/tumr (n/e/d), sysi/epon
proc, drug (D2/3/4/5/8/11)
Ankyrin: Long QT syndrome 4