Disease Directory

camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye is an extremely rare condition. Because few cases have been documented, detaile...

Camptodactyly-arthropathy-coxa vara-pericarditis syndrome (also known as CACP syndrome) is a rare genetic rheumatologic condition that primarily affec...

Camptodactyly-tall stature-scoliosis-hearing loss syndrome (CATSHL) is a very rare hereditary condition that primarily affects the skeleton, joints, s...

Camptodactyly-taurinuria syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Camptomelic syndrome, long-limb type is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cancer affecting the bone of the limb skeleton is a type of malignancy that involves the long bones of the arms or legs. It is a condition evaluated w...

Cancer of isthmus of fallopian tube is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cancer of long bone of lower limb is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cancer of long bone of upper limb is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cancer of short bone of lower limb is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cancer of short bone of upper limb is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cancer of unknown primary site is a term used when malignant tumors are identified by metastases, but the site of origin cannot be determined. It repr...

Cancer or benign tumor describes a group of conditions characterized by abnormal cell proliferation, which can lead to either malignant growths or non...

Cancer-associated retinopathy (CAR) is a paraneoplastic disorder linked to extraocular malignancies, characterized by the presence of autoantibodies a...

Candidemia is an invasive form of candidiasis in which species of candida are present in the blood, leading to a serious systemic infection. It most o...

Candidiasis, familial, 1 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Candidiasis, familial, 3 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Candidiasis, familial, 4 is a genetic condition caused by mutations in the CLEC7A gene, which is associated with chronic mucocutaneous candidiasis. Th...

Candidiasis, familial, 6, is a genetic condition caused by mutations in the IL17F gene. It is inherited in an autosomal dominant manner, meaning that...

Candidiasis, familial, 8 is a form of chronic mucocutaneous candidiasis caused by a mutation in the TRAF3IP2 gene. This condition primarily affects th...