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Rare Disease Database

Search Results for: G

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Also known as: galactose-1-phosphate uridylyl transferase deficiency, transferase deficiency galactosemia, GALT deficiency
Subdivisions: classic galactosemia, clinical variant galactosemia, biochemical variant galactosemia (Duarte variant galactosemia)

Galloway-Mowat Syndrome

Also known as: Galloway Syndrome, Hershberger Syndrome, Hiatal Hernia-Microcephaly-Nephrosis, Galloway Type, Microcephaly-Hiatal Hernia-Nephrosis, Galloway Type, Microcephaly-Hiatal Hernia-Nephrotic Syndrome, Nephrocerebellar Syndrome, Nephrosis-Microcephaly Syndrome, Nephrosis-Neuronal Dysmigration Syndrome, Yoder Dystonia


Also known as: delayed gastric emptying, gastric atony, gastric dysmotility, gastric stasis, gastrointestinal autonomic neuropathy, gastroparesis diabeticorum, gastropathy, severe functional dyspepsia
Subdivisions: diabetic gastroparesis, idiopathic gastroparesis, post-surgical gastroparesis

Gaucher Disease

Also known as: cerebroside lipidosis syndrome, Gaucher splenomegaly, glucocerebrosidase deficiency, glucocerebrosidosis, glucosylceramidase deficiency, glucosyl cerebroside lipidosis, kerasin lipoidosis, kerasin thesaurismosis, lipid histiocytosis (kerasin type), sphingolipidosis 1
Subdivisions: Gaucher disease type 1, Gaucher disease type 2, Gaucher disease type 3, perinatal-lethal form, cardiovascular form

General Myoclonus

Also known as: No synonyms found
Subdivisions: action myoclonus, arrhythmic myoclonus, cortical myoclonus, cortical-subcortical myoclonus, dyssynergia cerebellaris myoclonica, familial arrhythmic myoclonus, hereditary essential myoclonus, infantile myoclonic encephalopathy and polymyoclonia, intention myoclonus, Lance-Adams syndrome, myoclonic epilepsy, nocturnal myoclonus, opsoclonus, palatal myoclonus, paramyoclonus multiple, pathological myoclonus, peripheral myoclonus, postanoxic intention myoclonus, postencephalitic intention myoclonus, progressive myoclonic epilepsy, respiratory myoclonus, rhythmical myoclonus, segmental myoclonus, stimulus-sensitive myoclonus, subcortical/non-segmental myoclonus

Generalized Arterial Calcification of Infancy

Also known as: ENPP1 deficiency, ABCC6 deficiency, idiopathic infantile arterial calcification (IIAC), idiopathic arterial calcification of infancy (IACI), arterial calcification of infancy, occlusive infantile arterial calcification , occlusive infantile arteriopathy, GACI
Subdivisions: GACI type 1, GACI type 2

Geographic Tongue

Also known as: benign migratory glossitis, BMG, erythema areata migrans, erythema migrans, geographic stomatitis, wandering rash of the tongue

Gestational Trophoblastic Disease

Also known as: GTD, gestational trophoblastic neoplasia (GTN), malignant gestational trophoblastic disease, persistent gestational trophoblastic disease
Subdivisions: partial hydatiform mole, complete hydatiform mole, invasive mole, choriocarcinoma, placental site nodule (PSN), exaggerated placental site (EPS), placental site trophoblastic tumor (PSTT), epithelioid trophoblastic tumor (ETT)

Gianotti Crosti Syndrome

Also known as: Acrodermatitis, Infantile Lichenoid, Acrodermatitis, Papular Infantile, Crosti-Gianotti Syndrome, GCS, PAC, Papular Acrodermatitis of Childhood, PAS

Giant Cell Arteritis

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

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

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
Subdivisions: No subdivisions found

Gitelman Syndrome

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

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, GTA, platelet fibrinogen receptor deficiency, thrombasthenia, thrombasthenia of Glanzmann and Naegeli, integrin aIIbb3 deficiency of
Subdivisions: No subdivisions found


Also known as: glioblastoma multiforme, astrocytoma, grade IV, GBM


Also known as: glial tumor, glial cell tumor, glial neoplasm

Glucose-Galactose Malabsorption

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

Glutaric Aciduria Type I

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

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

Glycogen Storage Disease Type I

Also known as: glucose-6-phosphatase deficiency, glucose-6-phosphate transport defect, glycogenosis type I, GSDI, Von Gierke disease
Subdivisions: glycogen storage disease type IA, glycogen storage disease type IB

Glycogen Storage Disease Type III

Also known as: amylo-1,6-glucosidase deficiency, Cori disease, AGL deficiency, glycogenosis type III, Forbes disease, limited dextrinosis, GDE deficiency, glycogen debrancher deficiency, GSD-III

Glycogen Storage Disease Type IX

Also known as: GSD-IX, PhK deficiency, phosphorylase kinase deficiency
Subdivisions: glycogen storage disease type Ixa, glycogen storage disease type Ixb, glycogen storage disease type Ixc, glycogen storage disease type Ixd

Glycogen Storage Disease Type V

Also known as: Glycogenosis Type V, Glycogen Storage Disease type V (GSD-V), GSD-V, McArdle Disease, Myophosphorylase Deficiency, Muscle Glycogen Phosphorylase Deficiency

GNE Myopathy

Also known as: hereditary Inclusion body myopathy, HIBM, h-IBM, IBM2, inclusion body myopathy, autosomal recessive, inclusion body myopathy, quadriceps-sparing, QSM, hereditary inclusion body myopathy, distal myopathy with rimmed vacuoles, DMRV, Nonaka myopathy, rimmed vacuole myopathy, quadriceps sparing myopathy

Goblet Cell Carcinoid

Also known as: mucinous carcinoid, adenocarcinoid +/-ex GCC, goblet cell tumors (GCT), mucinous adenocarcinoids, microglandular-GCC, composite GCC-adenocarcinoma, mixed crypt cell carcinoma, adenocarcinoma ex GCC, appendiceal crypt cell adenocarcinoma, goblet cell carcinoma, GCC, goblet cell adenocarcinoid, goblet cell tumor

Gordon Syndrome

Also known as: arthrogryposis multiplex congenita, distal, type IIA, camptodactyly-cleft palate-clubfoot, distal arthrogryposis, type IIA

Gorlin-Chaudhry-Moss Syndrome

Also known as: Craniofacial Dysostosis-PD Arteriosus-Hypertrichosis-Hypoplasia of Labia, Craniosynostosis-Hypertrichosis-Facial and Other Anomalies, GCM Syndrome

Gottron Syndrome

Also known as: acrogeria, Gottron type, acrometageria, familial acrogeria, familial acromicria

Granuloma Annulare

Also known as: Lichen Annularis
Subdivisions: Generalized (Disseminated) Granuloma Annulare, Linear Granuloma Annulare, Localized Granuloma Annulare, Perforating Granuloma Annulare, Subcutaneous Granuloma Annulare

Granulomatosis with Polyangiitis

Also known as: GPA, midline granulomatosis, necrotizing respiratory granulomatosis, granulomatosis, Wegener’s disease (former), Wegener granulomatosis (former), Wegener’s granulomatosis (former)

Graves’ Disease

Also known as: Basedow disease, exophthalmic goiter, Graves' hyperthyroidism, Parry disease, toxic diffuse goiter
Subdivisions: Graves' dermopathy, Graves' orbitopathy, Graves' ophthalmopathy

Greig Cephalopolysyndactyly Syndrome

Also known as: frontodigital syndrome (obsolete), GCPS, Hootnick-Holmes syndrome (obsolete), polysyndactyly-dysmorphic craniofacies, Greig type, Cephalopolysyndactyly syndrome , Greig syndrome

Growth Hormone Insensitivity

Also known as: GHI, GH insensitivity, growth hormone resistance, growth hormone unresponsiveness, Laron syndrome
Subdivisions: GH inactivating antibodies, GH postreceptor deficiencies, GH receptor deficiency (GHRD)

Guillain-Barré Syndrome

Also known as: acute polyneuritis, acute inflammatory neuropathy, acute inflammatory polyneuropathy, GBS