Rare diseases

Rare diseases are among the hardest to diagnose. We believe medical doctors would benefit from an organised list of disorders from the disparate organisations and medical resources available. In the same way NORD and Eurodis provide information and support for patients, we collaborate with and provide information for health researchers and professionals. From here you can browse orphan, genetic or rare disorders along with summary statistics and links to further information.

Rare Diseases by name

Name
GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2	View info
GALLOWAY-MOWAT SYNDROME 3; GAMOS3	View info
GALLOWAY-MOWAT SYNDROME 4; GAMOS4	View info
GALLOWAY-MOWAT SYNDROME 5; GAMOS5	View info
GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO	View info
GAPO SYNDROME	View info
GASTRIC CANCER	View info
GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC	View info
GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID	View info
GAUCHER DISEASE, TYPE I	View info
GAUCHER DISEASE, TYPE II	View info
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1	View info
GELEOPHYSIC DYSPLASIA 1; GPHYSD1	View info
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1	View info
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2	View info
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7	View info
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9	View info
GENETIC HYPERFERRITINEMIA WITHOUT IRON OVERLOAD	View info
GENETIC TRANSIENT CONGENITAL HYPOTHYROIDISM	View info
GENITOPATELLAR SYNDROME; GTPTS	View info

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