Congenital Myotonia (CM) Congenital myotonia (CM) is a genetic neuromuscular disorder that is caused by diminished chloride conductance…gensolJune 10, 2025
Alpha-S1 Casein (CASEIN) Alpha-S1 Casein (CASEIN) is one of the four Casein proteins found in goat's milk and…gensolJune 10, 2025
Catalase Deficiency (CAT) Catalase Deficiency (CAT) is a genetic disorder that leads to reduced catalase enzyme activity which…gensolJune 5, 2025
Primary Open Angle Glaucoma Basset Fauve De Bretagne Type (POAG-4) Primary Open Angle Glaucoma Basset Fauve De Bretagne Type (POAG-4) is an inherited eye condition…gensolJune 5, 2025
Progressive Retinal Atrophy Rod-Cone Dysplasia 4 (PRA-RCD4) PRA-rcd4, Progressive Retinal Atrophy (rcd4-PRA), RCD4 Progressive Retinal Atrophy[email protected]May 8, 2024
Myxomatous Mitral Valve Disease (MMVD) Mitral Regurgitation, Degenerative Mitral Valve Disease, Endocardiosis[email protected]May 8, 2024