Rare Disease Database

Rare Disease Database

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Rare Disease Database GARD Rare Diseases Database
NORD Rare Disease Report
Giant Cell Arteritis

Also known as: cranial arteritis GCA granulomatous arteritis temporal arteritis (Horton's disease)

NORD Rare Disease Report
Giant Cell Myocarditis

Also known as: GCM idiopathic giant cell myocarditis

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NORD Rare Disease Report
Giant Congenital Melanocytic Nevus

Also known as: bathing trunk nevus cape nevus congenital pigmented nevus garment nevus giant brown birthmark giant hairy nevus giant hairy pigmented nevus giant mole giant nevus hairy birthmark leptomeningeal melanosis multiple congenital melanocytic nevi neurocutaneous melanocytosis neurocutaneous melanosis satellite nevi swimming trunk nevus

NORD Rare Disease Report
Gilbert Syndrome

Also known as: constitutional liver dysfunction familial nonhemolytic jaundice Gilbert-Lereboullet syndrome Gilbert's disease hyperbilirubinemia I Meulengracht's disease unconjugated benign bilirubinemia

NORD Rare Disease Report
Gitelman Syndrome

Also known as: familial hypokalemia-hypomagnesemia hypomagnesemia-hypokalemia with hypocalciuria

NORD Rare Disease Report
Glanzmann Thrombasthenia

Also known as: Glanzmann disease Glanzmann-Naegeli syndrome Glanzmann thrombasthenia Glanzmann thrombasthenia, type A glycoprotein complex IIb/IIIa, deficiency of GP IIb-IIIa complex, deficiency of GPIIb/IIIa receptor, deficiency of GTA platelet fibrinogen receptor deficiency thrombasthenia thrombasthenia of Glanzmann and Naegeli integrin αIIbβ3 receptor, deficiency of

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NORD Rare Disease Report
Glioblastoma

Also known as: glioblastoma multiforme astrocytoma, grade IV GBM

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NORD Rare Disease Report
Glioma

Also known as: glial tumor glial cell tumor glial neoplasm

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NORD Rare Disease Report
Glucose-Galactose Malabsorption

Also known as: monosaccharide malabsorption carbohydrate intolerance of glucose galactose complex carbohydrate intolerance GGM

NORD Rare Disease Report
Glutaric Aciduria Type I

Also known as: GA1 glutaric acidemia type I glutaric aciduria type I glutaryl-CoA dehydrogenase deficiency

NORD Rare Disease Report
Glutaric Aciduria Type II

Also known as: electron transfer flavoprotein, deficiency of electron transfer flavoprotein: ubiquinone oxidoreductase, deficiency of GAII Glutaric Acidemia II Glutaric Aciduria II GA2 Ethylmalonic adipic aciduria (EMA) MADD multiple acyl-Co-A dehydrogenase deficiency

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