Disease Directory

Conductive deafness-malformed external ear syndrome is a condition primarily affecting the structure of the external ear and the conductive mechanism...

Conductive deafness-ptosis-skeletal anomalies syndrome is a rare form of ectodermal dysplasia that primarily affects the development of the ears, eyel...

Cone dystrophy is an inherited ocular disorder characterized by the progressive loss of cone photoreceptor cells, which are essential for central and...

Cone dystrophy 3 is an inherited retinal condition that primarily affects the cone photoreceptors responsible for central and color vision. It is caus...

Cone dystrophy 4 is an inherited eye condition that primarily affects the cone cells in the retina, leading to visual disturbances such as reduced cla...

Cone dystrophy with supernormal rod response is an inherited retinal disorder that primarily affects the cone cells responsible for central vision and...

Cone dystrophy, X-linked, with tapetal-like sheen is an ocular condition that primarily affects the cone cells in the retina, which are responsible fo...

Cone-rod dystrophy (CRD) is a group of inherited retinal dystrophies characterized by progressive degeneration of the cone and rod photoreceptors in t...

Cone-rod dystrophy 1 is an inherited retinal condition that primarily affects the cone and rod cells responsible for central and peripheral vision. Al...

Cone-rod dystrophy 10 is an inherited retinal disorder that primarily affects the light-sensing cells of the retina, leading to visual impairment. It...

Cone-rod dystrophy 11 is an inherited disorder that affects the retina and impairs vision. It is caused by mutations in the RAX2 gene, which play a ke...

Cone-rod dystrophy 12 is an inherited eye condition that primarily affects the retina, leading to difficulties with color perception, central vision,...

Cone-rod dystrophy 13 is an inherited ocular condition that primarily affects the retina, leading to progressive visual loss and various vision abnorm...

Cone-rod dystrophy 14 is a condition affecting the retina, a light-sensitive layer at the back of the eye, which plays a crucial role in vision. Altho...

Cone-rod dystrophy 15 is a condition affecting the retina and leading to progressive visual loss. It is caused by mutations in the CDHR1 gene, which p...

Cone-rod dystrophy 16 is an inherited condition affecting the retina, where the cones and rods responsible for vision gradually lose their function. T...

Cone-rod dystrophy 17 is an inherited disorder affecting the retina, leading to visual impairment that may include difficulties with color perception...

Cone-rod dystrophy 18 is an inherited retinal disorder that primarily affects the photoreceptor cells responsible for color and low-light vision. It i...

Cone-rod dystrophy 19 is an inherited retinal disorder that affects both the cone and rod cells responsible for vision. It is caused by mutations in t...

Cone-rod dystrophy 2 is a rare inherited eye disorder caused by harmful changes in the CRX gene, which normally guides the growth and work of the reti...