Also known as: galactose-1-phosphate uridylyl transferase deficiency, transferase deficiency galactosemia, GALT deficiencySubdivisions: classic galactosemia, clinical variant galactosemia, biochemical variant galactosemia (Duarte variant galactosemia)
Also known as: delayed gastric emptying, gastric atony, gastric dysmotility, gastric stasis, gastrointestinal autonomic neuropathy, gastroparesis diabeticorum, gastropathy, severe functional dyspepsiaSubdivisions: diabetic gastroparesis, idiopathic gastroparesis, post-surgical gastroparesis
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 1Subdivisions: Gaucher disease type 1, Gaucher disease type 2, Gaucher disease type 3, perinatal-lethal form, cardiovascular form
Also known as: No synonyms foundSubdivisions: 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
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, GACISubdivisions: GACI type 1, GACI type 2
Also known as: GTD, gestational trophoblastic neoplasia (GTN), malignant gestational trophoblastic disease, persistent gestational trophoblastic diseaseSubdivisions: 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)
Also known as: constitutional liver dysfunction, familial nonhemolytic jaundice, Gilbert-Lereboullet syndrome, Gilbert's disease, hyperbilirubinemia I, Meulengracht's disease, unconjugated benign bilirubinemiaSubdivisions: No subdivisions found
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 ofSubdivisions: No subdivisions found
Also known as: glucose-6-phosphatase deficiency, glucose-6-phosphate transport defect, glycogenosis type I, GSDI, Von Gierke diseaseSubdivisions: glycogen storage disease type IA, glycogen storage disease type IB
Also known as: GSD-IX, PhK deficiency, phosphorylase kinase deficiencySubdivisions: glycogen storage disease type Ixa, glycogen storage disease type Ixb, glycogen storage disease type Ixc, glycogen storage disease type Ixd
Also known as: GVHDSubdivisions: Acute GVHD, Chronic GVHD
Also known as: Lichen AnnularisSubdivisions: Generalized (Disseminated) Granuloma Annulare, Linear Granuloma Annulare, Localized Granuloma Annulare, Perforating Granuloma Annulare, Subcutaneous Granuloma Annulare
Also known as: Basedow disease, exophthalmic goiter, Graves' hyperthyroidism, Parry disease, toxic diffuse goiterSubdivisions: Graves' dermopathy, Graves' orbitopathy, Graves' ophthalmopathy
Subdivisions: acquired GHD, congenital GHD, idiopathic GHD
Also known as: GHI, GH insensitivity, growth hormone resistance, growth hormone unresponsiveness, Laron syndromeSubdivisions: GH inactivating antibodies, GH postreceptor deficiencies, GH receptor deficiency (GHRD)