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
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2 Ge-Gh 3 Gi-Gl 4 Gm-Gp 5 Gq-Gt 6 Gu-Gz |
Ga-Gd
- 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
Ge-Gh
- 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
Gi-Gl
- 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
Gm-Gp
- 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
Gq-Gt
- 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
Gu-Gz
- 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
