Gerstmann Straussler Scheinker Disease |
Glycogen Storage Disease Type II |
Glycogen Storage Disease Type III |
Glycogen Storage Disease Type IV |
Glycogen Storage Disease Type V |
Globoid Cell Leukodystrophies |
Greig cephalopolysyndactyly syndrome |
Glutaric Acidemia I |
Gray Platelet Syndrome |
Glycogen Storage Disease Type IIb |
Goldberg-Shprintzen megacolon syndrome |
Glycogen Storage Disease Type VII |
Gamma-cystathionase deficiency |
Guanidinoacetate methyltransferase deficiency |
Gaucher Disease |
Gliomas |
Glomerulosclerosis, Focal Segmental |
Glycogen Storage Disease Type I |
Gitelman Syndrome |
Glycogen Storage Disease, Type IXD |
Glycine N-Methyltransferase Deficiency |
Glomerulosclerosis, Focal Segmental, 2 |
Griscelli syndrome type 1 |
Glanzmann Thrombasthenia, Autosomal Dominant |
Galactosemias |
Glycosuria, Renal |
Gout, HPRT-Related |
Glycogen Storage Disease IB |
Glucose-Galactose Malabsorption |
Gelatinous drop-like corneal dystrophy |
Growth-mental deficiency syndrome of Myhre |
Glucocorticoid-Remediable Aldosteronism |
Glucocorticoid Receptor Deficiency |
Glomus vagale tumors |
Glut1 Deficiency Syndrome |
Genitopatellar Syndrome |
Growth Deficiency and Mental Retardation with Facial Dysmorphism |
Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate |
Griscelli syndrome type 2 |
Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy |
Gerodermia osteodysplastica |
Gonadal dysgenesis XX type deafness |
Genee-Wiedemann syndrome |
Gonadal Dysgenesis, 46,XX |
Gordon syndrome |
Glutathione synthetase deficiency |
Glutamate formiminotransferase deficiency |
Groenouw type I corneal dystrophy |
Generalized Epilepsy With Febrile Seizures Plus, Type 2 |
Glycogen Storage Disease Type VI |
Glaucoma 1, Open Angle, A |
Glycogen Storage Disease 0, Liver |
Ghosal Hematodiaphyseal Dysplasia |
Glutamine deficiency, congenital |
Gracile bone dysplasia |
Glycogen Storage Disease IC |
Generalized Epilepsy With Febrile Seizures Plus, Type 1 |
Glycogen Storage Disease IXC |
Glaucomas |
Glaucoma, Open-Angle |
Glioblastoma |
Goiter |
Gangliosidosis, GM1 |
Glycogen Storage Disease XII |
Gamma aminobutyric acid transaminase deficiency |
Glutaric Aciduria III |
Glycogen Storage Disease IXB |
Glycinuria with or without Oxalate Urolithiasis |
Glaucoma 1, Open Angle, G |
Glomerulocystic Kidney Disease with Hyperuricemia and Isosthenuria |
Griscelli syndrome type 3 |
Gaucher Disease, Perinatal Lethal |
Glycogen Storage Disease of Heart, Lethal Congenital |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II |
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I |
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to |
Glaucoma 3, Primary Congenital, A |
Gaucher Disease, Type Iiic |
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to |
Glaucoma 1, Open Angle, F |
Gaucher Disease, Atypical, Due To Saposin C Deficiency |
Glomerulopathy With Fibronectin Deposits 2 |
Glaucoma 1, Open Angle, O |
Generalized Epilepsy With Febrile Seizures Plus, 7 |
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death |
Glycogen Storage Disease XIV |
Glycogen Storage Disease XIII |
Geleophysic dwarfism |
Generalized Epilepsy with Febrile Seizures Plus |
Giedion Langer Syndrome |
Goldmann-Favre Syndrome |
Great Vessels Transposition |
Glycosylphosphatidylinositol deficiency |
Glucocorticoid Deficiency 2 |
Glomerulonephritides, Membranoproliferative |
Glutathionuria |
Glucose Intolerance |
Galloway Mowat syndrome |
Glaucoma 3, Primary Congenital, D |
Glomerulopathy with fibronectin deposits |
Glomerulonephritides |
Gardner Syndrome |
Glomerulonephritides, IGA |
Glomerulonephritides, Membranous |
Giant Platelet Syndrome with Thrombocytopenia |
Generalized Epilepsy With Febrile Seizures Plus, Type 3 |
Glycoprotein IA Deficiency |
Gout |
Glucagonoma |
Gallstone |
Gastrinoma |
Gastrointestinal Hemorrhage |
Gonadal Dysgenesis |
Gonadal Dysgenesis, 46,XY |
Gains, Weight |
Giant Cell Tumor of Bone |
Gingival Overgrowth |
Granulosa cell tumor of the ovary |
Glaucoma 3, primary infantile, B |
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis |
GSD IV, Neuromuscular Form, Congenital |
GSD IV, Neuromuscular Form, Childhood |
Gallbladder Disease 4 |
Gm2-Gangliosidosis, Variant B1 |
Gastroesophageal Reflux |
Gonadal Dysgenesis, Mixed |
Gliosarcoma |
Gallbladder Neoplasm |
Gastrointestinal Neoplasm |
Guillain-Barre Syndrome |
Gastropareses |
Gestational Trophoblastic Disease |
Glioses |
Granulosa Cell Tumor |
Gland Neoplasm, Salivary |
Graves Ophthalmopathy |
Gorlin-Chaudhry-Moss syndrome |
Gambling |
Gastritides |
Gastroenteritides |
Gastroenteritides, Swine Transmissible |
Gingival Hyperplasia |
Gingival Hypertrophies |
Graft Occlusion, Vascular |
Granuloma, Plasma Cell |
Granuloma, Respiratory Tract |
Gynecomastia |
Genetic Translocations |
Goldenhar Syndrome |
Gastric Antral Vascular Ectasia |
Gait Disorder, Neurologic |
Genomic Instability |
Glucose Metabolism Disorder |
Granulocytopenia with Immunoglobulin Abnormality |
GSD IV, Neuromuscular Form, Fatal Perinatal |
Giant Axonal Neuropathy, Autosomal Dominant |
Glycogen Storage Disease IIIC |
Gastro-enteropancreatic neuroendocrine tumor |
Gaucher-like disease |
GEMSS syndrome |
Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to |
Galactorrhea |
Granuloma |
Graft Dysfunction, Primary |
Graft Rejection |
Ganglioglioma |
Gastroschisis |
Glaucoma-Related Pigment Dispersion Syndrome |
Gonadoblastoma |
Gliomas, Optic Nerve |
Ganglioneuroma |
Goiter, Nodular |
Gingivitides |
Glycogen Storage Disease Type Ix |
Gangrenes |
Glomus Jugulare Tumor |
Granuloma, Pyogenic |
Ganglioneuroblastoma |
Glossoptoses |
Gastric lymphoma |
Glycogen Storage Disease IIIA |
Giardiases |
Gingival Hemorrhage |
Gingival Recession |
Glaucoma, Neovascular |
Glossitides |
Glucose Tolerance Test |
Glycosuria |
Gestationi, Pemphigoid |
Growth hormone excess |
Gallbladder, Agenesis Of |
Gangliosidoses, GM2 |
Genu Varum |
Genu Valgum |
Gait Apraxia |
Glaucoma 1, Open Angle, E |
GSD IV, Classic Hepatic |
Geniospasm |
Glaucoma 1, Open Angle, D |
Glycogen Storage Disease IIIB |
Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement |
Glycogen Storage Disease, Type IXA2 |
Growth Hormone Deficiency With Pituitary Anomalies |
Gigantism |
Gonorrhea |
Gangliosidoses |
Giant Cell Tumor of Tendon Sheath |
Germinoma |
Granulomas, Periapical |
Gender Dysphoria |
Gastritis, Hypertrophic |
Granuloma, Lethal Midline |
Granuloma Annulare |
Gangrenes, Gas |
Glomus Tumor |
Glossalgia |
Gonadal Disorders |
Gastric Fistula |
Gerstmann Syndrome |
Gingival Neoplasm |
Gingivitis, Necrotizing Ulcerative |
Glycogen Storage Disease Type VIII |
Gnathostomiasis |
Giant Cell Granulomas |
Granuloma, Laryngeal |
Granulomatoses, Lymphomatoid |
Gland Calculi, Salivary |
Glioma, Subependymal |
Grover's disease |
Glycogen Storage Disease Id |
Granulomatous Mastitis |
Gurrieri Sammito Bellussi syndrome |
Glycoprotein Storage Disease |
Glaucoma 1, Open Angle, M |
Glassy cell carcinoma of the cervix |
Gestational Diabetes Insipidus |
Gigantiform Cementoma, Familial |
Gait |
Gallbladder |
Gamma Ray |
Ganglia |
Genitalia |
Growth |
Gland, Parathyroid |
Gland, Pituitary |
Gland, Salivary |
Gland, Sweat |
Gland, Thyroid |
Genitourinary Tract Anomalies |