Disease Directory

Bruck syndrome is a rare condition defined by the combination of osteogenesis imperfecta and congenital joint contractures. Osteogenesis imperfecta is...

Bruck syndrome 1 is a rare condition that occurs when there is a mutation in the FKBP10 gene. This mutation affects the way the body’s connective tiss...

Bruck syndrome 2 is a rare genetic disorder caused by a mutation in the PLOD2 gene. It is one form of Bruck syndrome and is also known by several name...

Brugada syndrome is a heart condition that affects the electrical system of the heart. It is characterized by an abnormal pattern on an electrocardiog...

Brugada syndrome 1 is a condition that affects the heart's rhythm and can lead to serious complications. It is defined as any Brugada syndrome in whic...

Brugada syndrome 2 is a rare condition that is a subtype of Brugada syndrome, where the cause of the disease is linked to a mutation in the GPD1L gene...

Brugada syndrome 3 is a rare heart condition that is part of the Brugada syndrome group. This condition occurs when there is a mutation in the CACNA1C...

Brugada syndrome 4 is a rare heart condition where a mutation in the CACNB2 gene causes abnormal heart rhythms. This disorder is one of several types...

Brugada syndrome 5 is a rare form of Brugada syndrome caused by a mutation in the SCN1B gene. This condition affects the heart's electrical system and...

Brugada syndrome 6 is a rare condition that is part of the Brugada syndrome group. In this condition, a mutation in the KCNE3 gene is the known cause....

Brugada syndrome 7 is a rare heart condition caused by a mutation in the SCN3B gene. This condition is a specific form of Brugada syndrome where the g...

Brugada syndrome 8 is a form of Brugada syndrome where the cause of the condition is known to be a mutation in the HCN4 gene. Brugada syndrome refers...

Brugada syndrome 9 is a form of Brugada syndrome, a rare heart condition that affects the heart's electrical activity. This variant is specifically li...

Brunner syndrome, also known as monoamine oxidase-A deficiency, is a very rare disorder that affects the way the body processes certain chemical messe...

Brunoni syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Bruton-type agammaglobulinemia, also known as X-linked agammaglobulinemia (XLA), is an inherited immunodeficiency disorder. It is called X-linked beca...

Budd-Chiari syndrome is a condition where the blood flow out of the liver is blocked. This blockage happens in the hepatic veins or the final part of...

Buratti-Harel syndrome is a rare condition noted in specialized databases such as OMIM and GARD. Detailed information about this syndrome is limited,...

Burkitt lymphoma is a rare form of malignant mature B-cell non-Hodgkin lymphoma that is characterized by very rapid growth. Research has shown that al...

Buschke Lowenstein tumor is a rare type of verrucous carcinoma that affects the skin or mucous membranes, primarily in the anogenital region. This typ...