Disease Directory

Weaver syndrome is a rare disorder that affects many parts of the body. It is mainly characterized by tall stature and a typical facial appearance, in...

Weaver-Williams syndrome is a rare condition that affects growth and development. It is a multiple congenital anomalies syndrome, meaning people with...

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

Weil's disease is a form of severe leptospirosis that causes jaundice, a condition in which the skin and eyes may turn yellow. This happens when the b...

Weill-Marchesani 4 syndrome, recessive is a rare genetic condition with several names including 15q26.3 microdeletion syndrome, WMS4, and Weill-Marche...

Weill-Marchesani syndrome (WMS) is a rare condition that affects the body’s structure. People with this syndrome often have short stature and distinct...

Weill-Marchesani syndrome 1 is a rare genetic condition caused by a mutation in the ADAMTS10 gene. This condition falls within the group of disorders...

Weill-Marchesani syndrome 2, dominant is a rare condition marked by several distinct features. It includes progressive stiffness in the joints, eye pr...

Weill-Marchesani syndrome 3 is a rare condition caused by a mutation in the LTBP2 gene. It is one type of Weill-Marchesani syndrome, a group of disord...

Weismann-Netter syndrome is a rare genetic condition that affects the bones. It is known as a primary bent bone dysplasia. People with this condition...

Weiss-Kruszka syndrome is a rare condition that has been identified through its association with the ZNF462 gene. The syndrome is also known by other...

Wells syndrome is a rare condition characterized by recurrent skin eruptions that resemble cellulitis along with an increase in eosinophils, a type of...

Werner syndrome is an inherited condition that causes many organs and tissues to age more quickly than usual, typically becoming apparent in late adol...

West-Nile encephalitis is an acute infection caused by a virus in the Flaviviridae family that is spread through the bite of an infected mosquito. In...

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

Whipple disease is a systemic infection caused by the Gram-positive bacterium Tropheryma whipplei. It primarily affects the small intestine, leading t...

Wieacker-Wolff syndrome is a severe neurodevelopmental disorder that primarily affects males and is characterized by significant contractures and inte...

Wieacker-Wolff syndrome (spectrum) is a rare disease. Detailed information about this condition is currently limited in medical literature.

Wieacker-Wolff syndrome, female-restricted is a rare condition that is mainly known to affect females. It is recognized as an X-linked dominant disord...

Wiedemann-Rautenstrauch syndrome is a very rare genetic condition that is recognized at birth. It is characterized by features that resemble premature...