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Saturday, October 11, 2008

List of rare diseases starting with G

This list of rare diseases was originally taken from the NIH public domain resource at http://ord.aspensys.com/asp/diseases/diseases.asp .

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

  • G syndrome
  • Galactocoele
  • Galactokinase deficiency
  • Galactorrhoea-Hyperprolactinaemia
  • Galactosamine-6-sulfatase deficiency
  • Galactose-1-phosphate uridyltransferase deficiency
  • 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
  • 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 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 Feinmesser Cohen syndrome
  • Geen Sandford Davison syndrome
  • Gelatinous ascites
  • Geleophysic dwarfism
  • Gelineau disease
  • Geliphobia
  • Gemignani syndrome
  • Gemss syndrome
  • 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
  • Gestational diabetes mellitus
  • Gestational pemphigoid
  • Gestational trophoblastic disease
  • Ghosal syndrome
  • Ghose Sachdev Kumar syndrome
  • 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
  • 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
  • Globel disaccharide intolerance
  • Glomerulonephritis sparse hair telangiectases
  • Glomerulonephritis
  • Glomerulosclerosis
  • Gloomy face syndrome
  • Glossodynia
  • Glossopalatine ankylosis micrognathia ear anomalies
  • Glossopharyngeal neuralgia
  • Glossophobia
  • 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
  • Glyceraldehyde-3-phosphate dehydrogenase deficiency
  • Glycine synthase deficiency
  • 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
  • GM2 gangliosidosis, 0 variant
  • GM2-gangliosidosis, B, B1, AB variant
  • Gms syndrome
  • Goldberg Bull syndrome
  • Goldberg syndrome
  • Goldblatt Wallis syndrome
  • Goldblatt Wallis Zieff syndrome
  • Goldblatt Viljoen syndrome
  • Goldenhar disease
  • 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
  • Goodman camptodactyly
  • Goodpasture pneumorenal syndrome
  • Goodpasture's syndrome
  • Gordon hyperkaliemia-hypertension syndrome
  • Gordon syndrome
  • Gorham syndrome
  • Gorham-Stout disease
  • Gorlin Bushkell Jensen syndrome
  • Gorlin Chaudhry Moss syndrome
  • Gottron's syndrome
  • Gougerot-Sjogren syndrome
  • Gouty nephropathy, familial
  • 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
  • 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
  • GTP cyclohydrolase deficiency
  • Guanidinoacetate methyltransferase deficiency
  • Guérin-Stern syndrome
  • Guibaud Vainsel syndrome
  • Guillain-Barre 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


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