X-linked myotubular myopathy | X-linked congenital stationary night blindness | secondary dominant | Phrygian dominant scale | Dominant seventh chord | Cross-linked polyethylene |
CHILD syndrome is inherited in an X-linked dominant fashion and is associated with a mutation of the NSDHL gene.
Mutations in the NSDHL gene are associated with CHILD syndrome which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males.