Joubert syndrome with ocular defect is a subtype of Joubert syndrome and related disorders. It is defined by the neurological features seen in Joubert...

Joubert syndrome with oculorenal defect is a rare subtype of Joubert syndrome and related disorders that affects the brain, kidneys, and eyes. It is a...

Joubert syndrome with renal defect is a rare subtype within the spectrum of Joubert syndrome and related disorders (JSRD). People with this condition...

Juberg-Hayward syndrome is a complex condition that involves multiple body systems. It is a polymalformative syndrome, meaning that people with this c...

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

Jugular foramen meningioma is a type of tumor that arises in the meninges at the level of the jugular foramen, a key opening at the base of the skull....

Junctional epidermolysis bullosa is a severe skin disorder primarily affecting the skin and mucosal membranes, where the layers of the skin separate e...

Junctional epidermolysis bullosa Herlitz type is a severe subtype of junctional epidermolysis bullosa marked by widespread blistering and erosions tha...

Junctional epidermolysis bullosa inversa, also known as EBJ-I or inverse JEB, is a rare and severe subtype of junctional epidermolysis bullosa that pr...

Junctional epidermolysis bullosa, non-Herlitz type is a subtype of junctional epidermolysis bullosa that primarily affects the skin and mucous membran...

Junctional epidermolysis bullosa with pyloric atresia is a severe disorder that primarily affects the skin and gastrointestinal system, characterized...

Juvenile absence epilepsy is a form of genetic epilepsy that generally presents around puberty and primarily affects the central nervous system. It is...

Juvenile arthritis due to defect in LACC1 is a rare form of juvenile arthritis that appears in children. The condition is linked to changes in the LAC...

Juvenile dermatitis herpetiformis is a condition that affects the skin of children, producing an itchy and blistering rash. The condition is character...

Juvenile dermatomyositis is a systemic, autoimmune inflammatory muscle disorder that primarily affects children, presenting with both muscle weakness...

Juvenile Huntington disease (JHD) is a rare neurodegenerative disorder characterized by the onset of symptoms before the age of 20. Although no specif...