Disease Index

Human disease

medical condition

human disease

human disease

medical condition

rare disease caused by prenatal exposure to valproic acid (VPA)

human disease

disease

human disease

astrocytoma that is characterized as a low grade astrocytoma and has material basis in neoplastic astrocytes

kidney disease

human disease

disease

Human disease

An extremely rare genetic condition where muscle and connective tissue gradually turn to bone, forming a second skeleton. Caused by mutations in the ACVR1 gene. Affects approximately 1 in 2 million people worldwide with no ethnic or geographical predisposition.

hepatocellular carcinoma characterized microscopically by laminated fibrous layers interspersed between the tumour cells. The polygonal, deeply eosinophilic tumor cells arise in non-cirrhotic livers

Fibronectin glomerulopathy is a hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life

connective tissue cancer that has material basis in fibrous connective tissue and characterized by the presence of immature proliferating fibroblasts or undifferentiated anaplastic spindle cells in a storiform pattern

human disease

bone remodeling disease that results in the destruction of normal bone and replacing it with fibrous bone tissue

human disease

human disease

Fibular dimelia-diplopodia syndrome is a rare developmental anomaly

congenital absence of the fibula

medical condition