Complex regional pain syndrome (CRPS) is a chronic condition primarily affecting the limbs, where individuals experience disproportionate pain often f...

Complex regional pain syndrome type 1 (CRPS1) is characterized by pain that is disproportionate to any known inciting event, often following an injury...

Complex regional pain syndrome type 2 (CRPS2), also known as causalgia, is characterized by severe, spontaneous pain following damage to a peripheral...

Composite hemangioendothelioma is an intermediate, locally aggressive blood vessel neoplasm that rarely metastasizes. Pathologically, it is characteri...

Composite lymphoma is a condition defined by the coexistence of Hodgkin lymphoma alongside non-Hodgkin lymphoma within the same anatomic site. It affe...

Compton-North congenital myopathy is a rare muscle condition that is known by several names including MYPCN, congenital lethal myopathy, and Compton-N...

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 is an inherited retinal condition classified among pigmentary retinopathies that primarily affects the photoreceptors in the eye. R...

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 disorder that primarily affects the retina, leading to a range of visual disturbances. It is caused by mutations...

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...