Disease Directory

Wolf-Hirschhorn syndrome is a rare genetic disorder that starts before birth and involves many parts of the body. It usually happens when a small sect...

Wolff-Parkinson-White syndrome is a heart condition that affects the way electrical signals travel through the heart. The condition is identified by a...

Wolffian duct adenocarcinoma is a type of cervical adenocarcinoma that develops from remnants of the mesonephric (Wolffian) ducts. This condition is c...

Wolfram syndrome, also known as DIDMOAD, is a neurodegenerative disorder that commonly presents with a combination of type I diabetes mellitus, diabet...

Wolfram syndrome 1 is an uncommon multi-system disorder that typically begins in childhood and affects the endocrine system, eyes, ears, kidneys, and...

Wolfram syndrome 2 is a multi-system condition caused by mutations in the CISD2 gene. It is characterized by the early onset of diabetes mellitus and...

Wolfram syndrome, mitochondrial form, is characterized by its mitochondrial and autosomal recessive inheritance patterns. While no specific genes have...

Wolfram-like syndrome is a rare endocrine condition that is mainly marked by a triad of symptoms including adult-onset diabetes mellitus, progressive...

Wolman disease is a rare condition that represents the most severe form of lysosomal acid lipase deficiency. This enzyme is important for breaking dow...

Woodhouse-Sakati syndrome is a multisystemic disorder that affects several parts of the body. It is characterized by a combination of signs including...

Worster-Drought syndrome is a type of cerebral palsy that affects the muscles of the face, especially the lips, tongue, and soft palate. This conditio...

Wyburn-Mason syndrome, also known as Bonnet-Dechaume-Blanc syndrome, is a rare condition characterized by abnormal connections between arteries and ve...

X small rings is a rare condition caused by a structural anomaly in the X chromosome. It shows a highly variable set of features among people, meaning...

X-linked Alport syndrome is a genetic condition that is noted as the X-linked form of Alport syndrome. This condition is linked with genetic changes t...

X-linked Ehlers-Danlos syndrome is a very rare form of the Ehlers-Danlos syndromes, a group of inherited connective tissue disorders. People with this...

X-linked Emery-Dreifuss muscular dystrophy is a form of muscular dystrophy that is inherited in an X-linked pattern. This means that the gene responsi...

X-linked Mendelian susceptibility to mycobacterial diseases is a rare group of immune system disorders. It is caused by specific mutations in the IKBK...

X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency is a rare condition caused by a mutation in the CYBB gene. This mut...

X-linked Opitz G/BBB syndrome is a rare genetic condition. It is defined as the X-linked form of Opitz G/BBB syndrome and is associated with changes i...

X-linked acrogigantism due to Xq26 microduplication is a rare genetic condition linked to changes on the X chromosome. The condition is known for its...