Disease Directory

Congenital pancreatic cyst is a very rare condition characterized by the presence of a fluid-filled cyst in the pancreas that is present from birth. I...

Congenital panfollicular nevus is a rare, benign skin tumor disorder that is present at birth. It is characterized by large, elevated, well-circumscri...

Congenital partial agenesis of pericardium is a rare congenital heart malformation characterized by the partial absence of the left pericardium. This...

Congenital partial pulmonary venous return anomaly, also known as Partial anomalous pulmonary Venous connection, is a heart condition in which one or...

Congenital patella dislocation is a musculoskeletal condition present from birth that affects the alignment of the kneecap. It is characterized by an...

Congenital patella dislocation, bilateral is a musculoskeletal condition characterized by an abnormal positioning of the kneecaps that is present at b...

Congenital patella dislocation, unilateral is a condition affecting the alignment of the kneecap on one side, present from birth. It is classified as...

Congenital patent ductus arteriosus aneurysm is a rare congenital anomaly involving an abnormal saccular dilatation of the ductus arteriosus. It prima...

Congenital pericardium anomaly describes a group of congenital cardiac malformations that affect the protective sac surrounding the heart. This condit...

Congenital plasminogen activator inhibitor type 1 deficiency is a rare bleeding disorder characterized by the premature breakdown of blood clots due t...

Congenital portosystemic shunt is a rare congenital anomaly affecting the great veins, where an abnormal connection allows portal blood to bypass the...

Congenital primary aphakia is an ocular condition present at birth that is characterized by the complete absence of the lens. It results from an arres...

Congenital primary lymphedema of Gordon is a rare condition affecting the lymphatic system, characterized by bilateral, painless swelling of the lower...

Congenital primary megaureter is an idiopathic condition affecting the urinary tract, where the ureter is abnormally dilated despite a normal bladder...

Congenital primary megaureter, nonrefluxing and unobstructed form is a condition that affects the urinary system, specifically involving an abnormally...

Congenital primary megaureter, obstructed form is a condition affecting the urinary system where the ureter, the tube that carries urine from the kidn...

Congenital primary megaureter, refluxing and obstructed form is a condition affecting the urinary tract, where the ureter is abnormally dilated, and b...

Congenital primary megaureter, refluxing form is a condition that affects the urinary tract, specifically involving an abnormally enlarged ureter with...

Congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome is a complex condition that affects multiple systems in...

Congenital prothrombin deficiency is an inherited bleeding disorder characterized by reduced activity of prothrombin, a key protein involved in blood...