HealthSignal
Rare conditions starting with G
Every condition in the NIH Genetic and Rare Diseases Information Center has its own HealthSignal community page, with condition information, stories, research and Signals sign-up.
175 conditions starting with G
- Gabriele de Vries syndrome
- Galactorrhoea-hyperprolactinaemia
- Galactosemia
- Galactosemia 4
- Galactosylceramide beta-galactosidase deficiency
- Gallbladder cancer
- Galloway-Mowat syndrome
- Gamma heavy chain disease (clinical)
- Gamma-aminobutyric acid transaminase deficiency
- Gamma-glutamylcysteine synthetase deficiency
- Gamma-Glutamyltransferase deficiency
- Gangliocytoma
- Ganglioglioma
- Gangliosidosis
- GAPO syndrome
- Gardner syndrome
- Gastric cancer
- Gastric mucosal hypertrophy
- Gastric non-hodgkin lymphoma
- Gastrocutaneous syndrome
- Gastrointestinal defects and immunodeficiency syndrome 1
- Gastrointestinal stromal tumor
- Gastroschisis
- Gaucher disease
- Gaucher disease perinatal lethal
- Gaucher disease type I
- Gaucher disease type II
- Gaucher disease type III
- GCGR-related hyperglucagonemia
- Gelatinous droplike corneal dystrophy
- Geleophysic dysplasia
- Gemignani syndrome
- Generalized basaloid follicular hamartoma syndrome
- Generalized dominant dystrophic epidermolysis bullosa
- Generalized epilepsy with febrile seizures plus
- Generalized epilepsy-paroxysmal dyskinesia syndrome
- Generalized junctional epidermolysis bullosa non-Herlitz type
- Generalized peeling skin syndrome
- Generalized pustular psoriasis
- Generalized resistance to thyroid hormone
- Genetic developmental and epileptic encephalopathy
- Geniculate herpes zoster
- Genito-palato-cardiac syndrome
- Genitopatellar syndrome
- Genochondromatosis
- Genochondromatosis type 1
- Genochondromatosis type 2
- Geroderma osteodysplastica
- Gerstmann syndrome
- Gerstmann-Straussler-Scheinker syndrome
- Gestational trophoblastic neoplasm
- Ghosal hematodiaphyseal dysplasia
- Giant axonal neuropathy
- Giant axonal neuropathy 1
- Giant axonal neuropathy 2
- Giant cell myocarditis
- Giant cell tumor of bone
- Gigantiform cementoma
- Gigantism
- Gillespie syndrome
- Gingival fibromatosis-facial dysmorphism syndrome
- Gingival fibromatosis-hypertrichosis syndrome
- Gingival fibromatosis-progressive deafness syndrome
- GJC2-related late-onset primary lymphedema
- Glanzmann thrombasthenia
- Glaucoma 1, open angle, A
- Glaucoma 3, primary infantile, B
- Glaucoma of childhood
- Glaucoma secondary to spherophakia/ectopia lentis and megalocornea
- Glaucoma type 1C
- Glaucoma-sleep apnea syndrome
- Glaucomatocyclitic crisis
- Glioblastoma
- Glioma
- Gliomatosis cerebri
- Gliosarcoma
- Global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome
- Global developmental delay-osteopenia-ectodermal defect syndrome
- Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome
- Glomerulonephritis
- Glomerulopathy with fibronectin deposits 1
- Glomerulopathy with fibronectin deposits 2
- Glomuvenous malformation
- Glossopalatine ankylosis
- Glossopharyngeal neuralgia
- Glucagonoma syndrome
- Glucocorticoid deficiency with achalasia
- Glucocorticoid resistance
- Glucocorticoid-remediable aldosteronism
- Glucose-6-phosphate transport defect
- GLUT1 deficiency syndrome
- Glutamate formiminotransferase deficiency
- Glutamate pyruvate transaminase 2 deficiency
- Glutaric aciduria, type 1
- Glutaryl-CoA oxidase deficiency
- Glycine encephalopathy
- Glycine N-methyltransferase deficiency
- Glycogen storage disease due to acid maltase deficiency, infantile onset
- Glycogen storage disease due to glucose-6-phosphatase deficiency type IA
- Glycogen storage disease due to lactate dehydrogenase deficiency
- Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
- Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
- Glycogen storage disease due to liver phosphorylase kinase deficiency
- Glycogen storage disease due to muscle and heart glycogen synthase deficiency
- Glycogen storage disease due to muscle beta-enolase deficiency
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- Glycogen storage disease IXb
- Glycogen storage disease IXd
- Glycogen storage disease type 1 due to SLC37A4 mutation
- Glycogen storage disease type III
- Glycogen storage disease type X
- Glycogen storage disease XV
- Glycogen storage disease, type I
- Glycogen storage disease, type II
- Glycogen storage disease, type IV
- Glycogen storage disease, type V
- Glycogen storage disease, type VI
- Glycogen storage disease, type VII
- Glycogen storage disorder due to hepatic glycogen synthase deficiency
- Glycosylphosphatidylinositol biosynthesis defect 15
- GM1 gangliosidosis
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM3 synthase deficiency
- GMS syndrome
- Gnathodiaphyseal dysplasia
- Gnathomiasis
- Gnb5-related intellectual disability-cardiac arrhythmia syndrome
- GNE myopathy
- GNPTG-mucolipidosis
- Goblet cell carcinoma
- Goldberg-Shprintzen syndrome
- Goldmann-Favre syndrome
- Gollop syndrome
- Gollop-Wolfgang complex
- Gomez Lopez Hernandez syndrome
- Gonadal dysgenesis
- Gonadotropin-independent familial sexual precocity
- Gonococcal conjunctivitis
- Gordon syndrome
- Gorham-Stout disease
- Gorlin syndrome
- GRACILE syndrome
- Grade III lymphomatoid granulomatosis
- Graham Little-Piccardi-Lassueur syndrome
- Graham-Boyle-Troxell syndrome
- Grange syndrome
- Grant syndrome
- Granular cell tumor
- Granulomatosis with polyangiitis
- Granulomatous amebic encephalitis
- Granulomatous slack skin disease
- Gray platelet syndrome
- Grayson-Wilbrandt corneal dystrophy
- Grebe syndrome
- Greenberg dysplasia
- Greig cephalopolysyndactyly syndrome
- Griscelli syndrome
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
- Groenouw corneal dystrophy type I
- Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
- Growth delay due to insulin-like growth factor I resistance
- Growth delay due to insulin-like growth factor type 1 deficiency
- Growth delay-hydrocephaly-lung hypoplasia syndrome
- Growth disorder
- Growth hormone insensitivity syndrome
- Growth retardation-mild developmental delay-chronic hepatitis syndrome
- Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy
- Grubben-de Cock-Borghgraef syndrome
- GTP cyclohydrolase I deficiency with hyperphenylalaninemia
- Guillain-Barre syndrome
- Guttmacher syndrome
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