Disease Directory

Wiedemann-Steiner syndrome is a rare genetic condition that primarily affects growth and neurodevelopment. Individuals with this condition typically p...

Wildervanck syndrome is a rare condition defined by a specific set of features. It is characterized by the fusion of cervical vertebrae (known as the...

Williams syndrome is a multisystem neurodevelopmental disorder that affects multiple parts of the body including the heart, connective tissue, and the...

Information about overview is currently limited for this condition.

Wilms tumor 1 is an autosomal disorder caused by changes in the WT1 gene. This condition increases the risk for Wilms tumor, a type of kidney cancer,...

Information about overview is currently limited for this condition.

Wilms tumor 3 is a rare condition that falls within the spectrum of Wilms tumors. Wilms tumors are generally types of kidney cancer that primarily aff...

Information about overview is currently limited for this condition.

Wilms tumor 5 is a rare form of Wilms tumor that occurs due to a mutation in the POU6F2 gene. This condition is one of several types of Wilms tumor an...

Wilms tumor 6 is a rare type of kidney tumor found in children. It is defined by the presence of a mutation in the REST gene. This mutation is the cau...

Information about overview is currently limited for this condition.

This condition is a subtype of WAGR syndrome that includes obesity along with other features such as Wilms tumor, aniridia (absence of the colored par...

Wilson disease is a very rare inherited condition that affects multiple organ systems, including the liver and central nervous system, due to abnormal...

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

Wilson-Turner syndrome is a very rare genetic condition affecting multiple systems, with a significant impact on cognitive and physical development. I...

Winchester syndrome is a rare genetic condition that is known by several names including MMP14-related multicentric osteolysis, nodulosis, and arthrop...

Wiskott-Aldrich syndrome is a primary immunodeficiency disorder that affects the immune system, blood, and skin. It is caused by mutations in the WAS...

Wiskott-Aldrich syndrome 2 is a condition caused by mutations in the WIPF1 gene that affects the immune system. Individuals with this condition typica...

Wiskott-Aldrich syndrome, autosomal dominant form is a condition that has been described in the medical literature, although detailed information rema...

Wolcott-Rallison syndrome is a very rare genetic condition. It is most known for causing permanent neonatal diabetes mellitus, which means that diabet...