Disease Directory

Gollop-Wolfgang complex is a very rare condition that affects the development of the limbs. In this condition, there is a significant malformation whe...

Gomez-Lopez-Hernandez syndrome is a very rare condition that belongs to a group of disorders known as neurocutaneous syndromes. This syndrome is noted...

Good syndrome, also known as thymoma-immunodeficiency, is a very rare adult-onset condition that combines a tumor in the thymus (thymoma) with a weake...

Goodman syndrome is an extremely rare genetic disorder that has been described in the medical literature since 1979. This condition is characterized b...

Gordon syndrome is an extremely rare condition that involves multiple congenital malformations. It is mainly characterized by contractures of the hand...

Gorham-Stout disease is a rare condition marked by the loss of bone (osteolysis) associated with the growth and enlargement of lymphatic vessels. It c...

Graham Little-Piccardi-Lassueur syndrome is a rare skin condition that is considered a variant of lichen planopilaris. It is known by several names in...

Graham-Boyle-Troxell syndrome, also known as cystic hamartoma of lung and kidney, is a very rare developmental malformation. It was reported in only t...

Grant syndrome is a rare disorder that shows similarities to osteogenesis imperfecta. It was first described in two patients and is marked by several...

Grayson-Wilbrandt corneal dystrophy (GWCD) is an extremely rare eye condition that affects the cornea, which is the clear outer layer of the eye. In t...

Greenberg dysplasia is a very rare and lethal skeletal disorder that affects fetal development. It is marked by the presence of fetal hydrops, very sh...

Greig cephalopolysyndactyly syndrome (GCPS) is a condition that involves multiple congenital anomalies. It is described as a pleiotropic syndrome, mea...

Information about this rare condition is currently limited. Greig cephalopolysyndactyly-contiguous gene syndrome is a condition that has been recogniz...

Griscelli syndrome is a rare condition that mainly affects a person's hair and skin. People with this condition often have a silvery gray sheen to the...

Griscelli syndrome type 1 is a rare genetic condition that is mainly characterized by a silvery gray sheen to the hair and lighter skin pigmentation c...

Griscelli syndrome type 2 (GS2) is a rare genetic condition that affects the skin, hair, and immune system. People with this condition typically have...

Griscelli syndrome type 3 is a rare condition that mainly affects the pigmentation of hair and skin. People with this condition typically have a silve...

Information about overview is currently limited for this condition.

Grubben-de Cock-Borghgraef syndrome is a rare intellectual disability syndrome. It is characterized by pre- and postnatal growth deficiency and genera...

Guillain-Barre syndrome is a spectrum of uncommon post-infectious neuropathies that primarily affect the peripheral nerves. It encompasses several var...