Disease Directory

Hepatosplenic T-cell lymphoma is an aggressive form of extranodal non-Hodgkin lymphoma that originates from mature cytotoxic T-cells, most often of th...

Hereditary North American Indian childhood cirrhosis is a severe liver condition that has been seen in aboriginal children from northwestern Quebec. I...

Hereditary acrokeratotic poikiloderma, Weary type is a condition characterized by distinctive skin changes that may include alterations in pigmentatio...

Hereditary amyloidosis is a group of inherited conditions characterized by the deposition of an abnormal protein called amyloid in multiple organs, mo...

Hereditary anemia is an inherited blood disorder that affects red blood cell production and function. It is associated with alterations in several gen...

Hereditary angioedema is a genetic condition characterized by recurrent episodes of swelling that can affect the skin and mucosal tissues, sometimes r...

Hereditary angioedema type 1 (HAE 1) is characterized by episodes of acute swelling in subcutaneous tissues, the gastrointestinal tract, and/or the up...

Hereditary angioedema type 2 (HAE 2) is a rare genetic condition characterized by recurrent episodes of severe swelling in various parts of the body,...

Hereditary angioedema type 3 is a form of hereditary angioedema characterized by recurrent episodes of acute swelling in the subcutaneous tissues, vis...

Hereditary angioedema with C1Inh deficiency is a rare condition that affects the regulation of inflammation due to mutations in the SERPING1 gene, whi...

Hereditary angioedema with normal C1Inh is a rare condition characterized by unpredictable, potentially life-threatening episodes of swelling without...

Hereditary angioedema with normal C1inh not related to F12 or PLG variant is a condition characterized by recurrent episodes of swelling that can affe...

Hereditary anorectal anomalies are congenital conditions that affect the development and structure of the anorectal region. Although the precise genet...

Hereditary antithrombin deficiency is a rare, genetic hematological condition characterized by reduced antithrombin activity, which impairs the normal...

Hereditary ataxia is an atactic disorder characterized by difficulties with coordination and balance that arise from an inherited genomic modification...

Hereditary benign intraepithelial dyskeratosis is an extremely rare inherited disorder that typically presents in early childhood. The condition is ch...

Hereditary breast carcinoma is a form of breast cancer that occurs in individuals with a family history of the disease. It is linked to inherited vari...

Hereditary breast ovarian cancer syndrome is a condition that significantly increases the risk of developing cancers such as breast, ovarian, and othe...