Scroll Search Results for: G Also known as: galactose-1-phosphate uridylyl transferase deficiency, transferase deficiency galactosemia, GALT deficiency 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: Idiopathic Chronic, Erosive Gastritis, Varioliform Gastritis Also known as: Gastroenteropathy, Protein Losing, Giant Hypertrophy of the Gastric Mucosa, Hypertrophic Gastropathy Also known as: GIST Also known as: delayed gastric emptying, gastric atony, gastric dysmotility, gastric stasis, gastrointestinal autonomic neuropathy, gastroparesis diabeticorum, gastropathy, severe functional dyspepsia Also known as: congenital fissure , laparoschisis 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 Also known as: No synonyms found 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 Also known as: benign migratory glossitis, BMG, erythema areata migrans, erythema migrans, geographic stomatitis, wandering rash of the tongue Also known as: Developmental Gerstmann Syndrome, Gerstmann Tetrad, GS Also known as: Gerstmann-Sträussler-Scheinker (GSS) syndrome, GSS Also known as: GTD, gestational trophoblastic neoplasia (GTN), malignant gestational trophoblastic disease, persistent gestational trophoblastic disease Also known as: Acrodermatitis, Infantile Lichenoid, Acrodermatitis, Papular Infantile, Crosti-Gianotti Syndrome, GCS, PAC, Papular Acrodermatitis of Childhood, PAS Also known as: GAN Also known as: cranial arteritis, GCA, granulomatous arteritis, temporal arteritis (Horton's disease) Also known as: GCM, idiopathic giant cell myocarditis 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 Also known as: constitutional liver dysfunction, familial nonhemolytic jaundice, Gilbert-Lereboullet syndrome, Gilbert's disease, hyperbilirubinemia I, Meulengracht's disease, unconjugated benign bilirubinemia Also known as: familial hypokalemia-hypomagnesemia, hypomagnesemia-hypokalemia with hypocalciuria 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 Also known as: glioblastoma multiforme, astrocytoma, grade IV, GBM Also known as: glial tumor, glial cell tumor, glial neoplasm Also known as: De Vivo Disease, glucose transporter protein syndrome, Glut1 deficiency syndrome, Glut1DS Also known as: G6PD deficiency, G6PD Also known as: monosaccharide malabsorption, carbohydrate intolerance of glucose galactose, complex carbohydrate intolerance, GGM Also known as: GA1, glutaric acidemia type I, glutaric aciduria type I, glutaryl-CoA dehydrogenase deficiency 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 Also known as: Pyroglutamicaciduria, Pyroglutamic Aciduria, 5-Oxoprolinuria Also known as: GSD7, muscle phosphofructokinase deficiency, PFKM Deficiency, Tarui disease Also known as: glucose-6-phosphatase deficiency, glucose-6-phosphate transport defect, glycogenosis type I, GSDI, Von Gierke disease 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 Also known as: GSD-IX, PhK deficiency, phosphorylase kinase deficiency Also known as: Glycogenosis Type V, Glycogen Storage Disease type V (GSD-V), GSD-V, McArdle Disease, Myophosphorylase Deficiency, Muscle Glycogen Phosphorylase Deficiency Also known as: Hers disease, liver phosphorylase deficiency, phosphorylase deficiency glycogen storage disease, GDS6 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 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 Also known as: Pneumorenal Syndrome Also known as: arthrogryposis multiplex congenita, distal, type IIA, camptodactyly-cleft palate-clubfoot, distal arthrogryposis, type IIA Also known as: Craniofacial Dysostosis-PD Arteriosus-Hypertrichosis-Hypoplasia of Labia, Craniosynostosis-Hypertrichosis-Facial and Other Anomalies, GCM Syndrome Also known as: acrogeria, Gottron type, acrometageria, familial acrogeria, familial acromicria Also known as: GVHD Also known as: Lichen Annularis Also known as: GPA, midline granulomatosis, necrotizing respiratory granulomatosis, granulomatosis, Wegener’s disease (former), Wegener granulomatosis (former), Wegener’s granulomatosis (former) Also known as: Basedow disease, exophthalmic goiter, Graves' hyperthyroidism, Parry disease, toxic diffuse goiter Also known as: frontodigital syndrome (obsolete), GCPS, Hootnick-Holmes syndrome (obsolete), polysyndactyly-dysmorphic craniofacies, Greig type, Cephalopolysyndactyly syndrome , Greig syndrome Also known as: TAD, Transient Acantholytic Dermatosis Also known as: GHI, GH insensitivity, growth hormone resistance, growth hormone unresponsiveness, Laron syndrome Also known as: GAMT deficiency Also known as: acute polyneuritis, acute inflammatory neuropathy, acute inflammatory polyneuropathy, GBS 
