List of diseases (G)
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Diseases |
G
Ga
Gal-Gap
- Galactorrhea
- Galactocoele
- Galactokinase deficiency
- Galactorrhoea-Hyperprolactinaemia
- Galactosamine-6-sulfatase deficiency
- Galactose-1-phosphate uridyltransferase deficiency
- Galactosemia
- Galloway Mowat syndrome
- Gamborg Nielsen syndrome
- Game Friedman Paradice syndrome
- Gamma aminobutyric acid transaminase deficiency
- Gamma-cystathionase deficiency
- Gamma-sarcoglycanopathy
- Gamstorp episodic adynamy
- Ganglioglioma
- Gangliosidosis (Type2)(GM2)
- Gangliosidosis GM1 type 3
- Gangliosidosis type1
- GAPO syndrome
Gar-Gau
- Garcia Torres Guarner syndrome
- Gardner Morrisson Abbot syndrome
- Gardner Silengo Wachtel syndrome
- Gardner-Diamond syndrome
- Gardner's syndrome
- Garret Tripp syndrome
- Gas/bloat syndrome
- Gastric Dumping Syndrome
- Gastric lymphoma
- Gastritis, familial giant hypertrophic
- Gastrocutaneous syndrome
- Gastroenteritis, eosinophilic
- Gastro-enteropancreatic neuroendocrine tumor
- Gastroesophageal reflux
- Gastrointestinal autonomic nerve tumor
- Gastrointestinal neoplasm
- Gaucher disease type 1
- Gaucher disease type 2
- Gaucher disease type 3
- Gaucher Disease
- Gaucher ichthyosis restrictive dermopathy
- Gaucher-like disease
- Gaucher's disease
Gay
Ge
Gee-Gem
- Geen Sandford Davison syndrome
- Gelatinous ascites
- Geleophysic dwarfism
- Gelineau disease
- Geliphobia
- Gemignani syndrome
- Gemss syndrome
Gen-Ger
- Genée-Wiedemann syndrome
- Generalized malformations in neuronal migration
- Generalized resistance to thyroid hormone
- Generalized seizure
- Generalized torsion dystonia
- Genes syndrome
- Genetic Diseases, Inborn
- Genetic reflex epilepsy
- Genetic susceptibility to infections caused by BCG
- Geniophobia
- Genital anomaly cardiomyopathy
- Genital dwarfism, Turner type
- Genital dwarfism
- Genito palatocardiac syndrome
- Genu valgum, st. Helena familial
- Genu varum
- Genuphobia
- Geographic tongue
- German syndrome
- Germinal cell aplasia
- Gerodermia osteodysplastica
- Gershinibaruch Leibo syndrome
- Gerstmann syndrome
Ges
Gh
Gi
- Gianotti-Crosti syndrome
- Giant axonal neuropathy
- Giant cell arteritis
- Giant cell myocarditis
- Giant congenital nevi
- Giant ganglionic hyperplasia
- Giant hypertrophic gastritis
- Giant mammary hamartoma
- Giant papillary conjunctivitis
- Giant pigmented hairy nevus
- Giant platelet syndrome
- Giardiasis
- Giedion syndrome
- Gigantism advanced bone age hoarse cry
- Gigantism partial, nevi, hemihypertrophy, macrocephaly
- Gigantism
- Gilbert's syndrome
- Gilles de la Tourette's syndrome
- Gingival fibromatosis dominant
- Gingival fibromatosis facial dysmorphism
- Gingival fibrosis
- Gingivitis
- Girate atrophy of choroid and retina
- Gitelman syndrome
- Gittings syndrome
Gl
Gla-Gli
- Glanzmann thrombasthenia
- Glass Chapman Hockley syndrome
- Glaucoma ecopia microspherophakia stiff joints short stature
- Glaucoma iridogoniodysgenesia
- Glaucoma sleep apnea
- Glaucoma type 1C
- Glaucoma, congenital
- Glaucoma, hereditary adult type 1A
- Glaucoma, hereditary juvenile type 1B
- Glaucoma, hereditary
- Glaucoma, primary infantile type 3A
- Glaucoma, primary infantile type 3B
- Glioblastoma multiforme
- Glioblastoma
- Glioma
- Gliomatosis cerebri
- Gliosarcoma
Glo
- Globel disaccharide intolerance
- Glomerulonephritis sparse hair telangiectases
- Glomerulonephritis
- Glomerulosclerosis
- Gloomy face syndrome
- Glossodynia
- Glossopalatine ankylosis micrognathia ear anomalies
- Glossopharyngeal neuralgia
- Glossophobia
Glu
- Glucagonoma
- Glucocorticoid deficiency, familial
- Glucocorticoid resistance
- Glucocorticoid sensitive hypertension
- Glucose 6 phosphate dehydrogenase deficiency
- Glucose-6-phosphate translocase deficiency
- Glucose-galactose malabsorption
- Glucosephosphate isomerase deficiency
- Glucosidase acid-1,4-alpha deficiency
- Glut2 deficiency
- Glutamate decarboxylase deficiency
- Glutamate-aspartate transport defect
- Glutaricaciduria I
- Glutaricaciduria II
- Glutaryl-CoA dehydrogenase deficiency
Gly
- Glyceraldehyde-3-phosphate dehydrogenase deficiency
- Glycine synthase deficiency
- Glycogen storage disease
- Glycogen storage disease type 1B
- Glycogen storage disease type 1C
- Glycogen storage disease type 1D
- Glycogen storage disease type 6, due to phosphorylation
- Glycogen storage disease type 7
- Glycogen storage disease type 9
- Glycogen storage disease type II
- Glycogen storage disease type V
- Glycogen storage disease type VI
- Glycogen storage disease type VII
- Glycogen storage disease type VIII
- Glycogenosis type II
- Glycogenosis type III
- Glycogenosis type IV
- Glycogenosis type V
- Glycogenosis type VI
- Glycogenosis type VII
- Glycogenosis type VIII
- Glycogenosis, type 0
- Glycosuria
Gm
Go
Gol-Gon
- Goldberg Bull syndrome
- Goldberg syndrome
- Goldblatt Wallis syndrome
- Goldblatt Wallis Zieff syndrome
- Goldblatt Viljoen syndrome
- Goldenhar syndrome
- Goldskag Cooks Hertz syndrome
- Goldstein Hutt syndrome
- Gollop Coates syndrome
- Gollop syndrome
- Goltz syndrome
- Gombo syndrome
- Gomez and López-Hernández syndrome
- Gonadal dysgenesis mixed
- Gonadal dysgenesis Turner type
- Gonadal dysgenesis XY type associated anomalies
- Gonadal dysgenesis, XX type
- Gonadal dysgenesis, XY female type
- Gonadal dysgenesis
- Goniodysgenesis mental retardation short stature
- Gonococcal conjunctivitis
- Gonzales Del Angel syndrome
Goo-Gou
- Goodman camptodactyly
- Goodpasture pneumorenal syndrome
- Goodpasture's syndrome
- Gordon hyperkaliemia-hypertension syndrome
- Gordon syndrome
- Gorham syndrome
- Gorham's disease
- Gorham-Stout disease
- Gorlin Bushkell Jensen syndrome
- Gorlin Chaudhry Moss syndrome
- Gottron's syndrome
- Gougerot-Blum syndrome
- Gougerot-Sjogren syndrome
- Gouty nephropathy, familial
Gr
Gra-Gri
- Graft versus host disease
- Graham Boyle Troxell syndrome
- Grand Kaine Fulling syndrome
- Grant syndrome
- Granulocytopenia
- Granuloma annulare
- Granulomas, congenital cerebral
- Granulomatosis, lymphomatoid
- Granulomatous allergic angiitis
- Granulomatous hypophysitis
- Granulomatous rosacea
- Graphite Pneumoconiosis
- Graves' disease
- Gray platelet syndrome
- Great vessels transposition
- Greenberg dysplasia
- Greig cephalopolysyndactyly syndrome GCPS
- Griscelli disease
- Grix Blankenship Peterson syndrome
Gro-Gru
- Groll Hirschowitz syndrome
- Grosse syndrome
- Grover's disease
- Growth deficiency brachydactyly unusual facies
- Growth delay, constitutional
- Growth hormone deficiency
- Growth mental deficiency syndrome of Myhre
- Growth retardation alopecia pseudoanodontia optic
- Growth retardation hydrocephaly lung hypoplasia
- Growth retardation mental retardation phalangeal hypoplasia
- Grubben Decock Borghgraef syndrome
Gt-Gy
- GTP cyclohydrolase deficiency
- Guanidinoacetate methyltransferase deficiency
- Guérin-Stern syndrome
- Guibaud Vainsel syndrome
- Guillain-Barré syndrome
- Guizar Vasquez Luengas syndrome
- Guizar Vasquez Sanchez Manzano syndrome
- Gunal Seber Basaran syndrome
- Gupta Patton syndrome
- Gurrieri Sammito Bellussi syndrome
- Gusher syndrome
- Gymnophobia
- Gyrate atrophy of the retina
- Gyrate atrophy
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
