Gaucher disease perinatal lethal is a severe, multisystem disorder affecting the blood and immune system, growth, and respiratory function. It is the...

Gaucher disease type I is a chronic, non-neurological form of Gaucher disease characterized primarily by organomegaly, bone involvement, and cytopenia...

Gaucher disease type II is the acute neuronopathic form of Gaucher disease, affecting multiple body systems but especially the brainstem and other neu...

Gaucher disease type III is the subacute neurological form of Gaucher disease, characterized by progressive encephalopathy along with systemic manifes...

GCGR-related hyperglucagonemia is a rare condition affecting the pancreas. It is caused by mutations in the GCGR gene and is characterized by an overg...

Gelatinous drop-like corneal dystrophy is a superficial corneal disorder characterized by the development of multiple prominent milky-white gelatinous...

Geleophysic dysplasia is a rare skeletal dysplasia that primarily affects bone and connective tissue development. Individuals with this condition typi...

Gemignani syndrome is a rare condition that is also known as spinocerebellar ataxia-amyotrophy-deafness syndrome or spinocerebellar ataxia associated...

Gemistocytic astrocytoma is a rare variant of diffuse astrocytoma that arises in the brain and is defined by the presence of a significant proportion...

Generalized dominant dystrophic epidermolysis bullosa is a subtype of dystrophic epidermolysis bullosa that primarily affects the skin, leading to wid...

Generalized dystonia is a movement disorder characterized by involuntary muscle contractions and abnormal postures, often affecting multiple parts of...

Generalized epilepsy-paroxysmal dyskinesia syndrome is a neurological condition marked by the coexistence of generalized epilepsy, which often present...

Generalized epilepsy with febrile seizures plus is a familial epilepsy syndrome characterized by a spectrum of seizure types, ranging from simple febr...