Disease Directory

Benign partial epilepsy of infancy with complex partial seizures is an extremely rare condition. Because few cases have been documented, detailed clin...

Benign partial epilepsy with secondarily generalized seizures in infancy is an extremely rare condition. Because few cases have been documented, detai...

benign partial infantile seizures is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Benign peripheral nerve granular cell tumor is an extremely rare condition. Because few cases have been documented, detailed clinical information is l...

benign peripheral nerve sheath tumor is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Benign prostate phyllodes tumor is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Benign recurrent intrahepatic cholestasis (BRIC) is a hereditary liver disorder characterized by intermittent episodes of cholestasis, which is the im...

Benign recurrent intrahepatic cholestasis type 1 (BRIC1) is a genetic condition characterized by intermittent episodes of liver dysfunction known as c...

Benign recurrent intrahepatic cholestasis type 2 (BRIC2) is primarily associated with variants in the ABCB11 gene, which encodes a bile salt export pu...

Benign skeletal muscle neoplasm is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

benign struma ovarii is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

benign teratoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Benign testicular sertoli cell tumor is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Benign thyroid gland neoplasm is a non-cancerous growth arising from the thyroid gland. This condition is not linked to any known genetic alterations...

Bent bone dysplasia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Bent bone dysplasia syndrome 1 is a skeletal dysplasia characterized by significant abnormalities in bone formation and structure. The condition is ca...

Bent bone dysplasia syndrome 2 is a complex condition that predominantly affects the skeletal system, leading to multiple bone and joint abnormalities...

Beta thalassemia is a blood disorder characterized by a deficiency or absence in the production of beta globin chains, which are essential for forming...

Beta-ketothiolase deficiency is an inherited metabolic disorder that disrupts the normal processing of ketone bodies and the catabolism of the amino a...

Beta-mannosidosis is a very rare lysosomal storage disorder that interferes with how cells break down certain complex sugars, leading to multi-system...