List of rare diseases-G
NIH genetic and rare disease info[edit source]
List of rare diseases-G is a rare disease.
- G syndrome
- G1D
- G6P translocase deficiency
- G6PD deficiency
- GA 1
- GA 2
- GA III
- GABA metabolic defect
- GABA transaminase deficiency
- GABAT
- GABEB
- Gabrielli syndrome
- Gaisboeck's syndrome
- Gait ataxia with late onset polyneuropathy syndrome
- Gait disorder antibody late-age onset polyneuropathy
- Gait disorder, autoantibody to a neural antigen, late-age onset, and polyneuropathy
- Galactocele
- Galactocerebrosidase deficiency
- Galactocoele
- Galactokinase deficiency
- Galactokinase deficiency galactosemia
- Galactorrhea amenorrhea without pregnancy
- Galactorrhea-Hyperprolactinemia
- Galactorrhoea-Hyperprolactinaemia
- Galactosamine-6-sulfatase deficiency
- Galactose epimerase deficiency
- Galactose-1-phosphate uridyl transferase deficiency
- Galactose-1-phosphate uridyltranferase deficiency
- Galactose-1-phosphate uridyltransferase deficiency
- Galactose-1-phosphate uridyl-transferase deficiency disease
- Galactosemia
- Galactosemia 2
- Galactosemia 3
- Galactosemia type 1
- Galactosemia type 2
- Galactosemia type 3
- Galactosemia, classic
- Galactosialidosis
- Galactosylceramide beta-galactosidase deficiency
- Galactosyltransferase 1 deficiency
- GALC deficiency
- GALE deficiency
- GALE-D
- Galen vein aneurysm
- Galenic arteriovenous malformation
- GALK deficiency
- GALK-D
- Gallbladder cancer
- Gallbladder, left-sided
- Galloway Mowat syndrome
- Galloway syndrome
- Galloway-Mowat syndrome
- Gallstone cholecystitis
- GALNS deficiency
- GALOP syndrome
- GALT deficiency
- Gambian sleeping sickness
- Game Friedman Paradice syndrome
- Game-Friedman-Paradice syndrome
- Gamma aminobutyrate transaminase deficiency
- Gamma aminobutyric acid transaminase deficiency
- Gamma heavy chain deposition disease
- Gamma heavy chain disease
- Gamma-A-globulin, selective deficiency of- not a rare disease.
- Gamma-cystathionase deficiency
- Gammaglobulin Deficiency
- Gamma-glutamyltransferase deficiency
- Gamma-glutamyltranspeptidase deficiency
- Gamma-hydroxybutyricaciduria
- Gamma-sarcoglycanopathy
- Gamstorp disease
- Gamstorp episodic adynamy
- Gamstorp-Wohlfart Syndrome
- GAMT deficiency
- GAN
- GAN1
- Gangliocytoma
- Ganglioglioma
- Ganglioside neuraminidase deficiency
- Ganglioside sialidase deficiency
- Gangliosidosis
- Gangliosidosis generalized GM1 chronic type
- Gangliosidosis generalized GM1 infantile form
- Gangliosidosis generalized GM1 juvenile type
- Gangliosidosis generalized GM1 type 1
- Gangliosidosis generalized GM1 type 2
- Gangliosidosis GM1 type 3
- Gangliosidosis GM2 , type 1
- GAPDH deficiency
- GAPO syndrome
- Garcia-Lurie syndrome
- Gardner syndrome
- Gardner-Diamond syndrome
- Gardner's syndrome
- Gardner-Silengo-Wachtel syndrome
- Gareis-Mason syndrome
- Garret Tripp syndrome
- GAS
- Gas bloat syndrome
- Gastric antral vascular ectasia
- Gastric cancer
- Gastric cancer, familial diffuse
- Gastric cancer, hereditary diffuse
- Gastric duplication cysts
- Gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma
- Gastric lymphoma
- Gastric Non-Hodgkin Lymphoma
- Gastrinoma
- Gastrocutaneous syndrome
- Gastro-enteropancreatic neuroendocrine tumor
- Gastroenteropathy, protein losing
- Gastroesophageal laceration-hemorrhage
- Gastrointestinal autonomic nerve tumor
- Gastrointestinal Stromal Sarcoma
- Gastrointestinal Stromal Tumors
- Gastroparesis
- Gastroschisis
- GATA2 deficiency
- GATAD2B-associated neurodevelopmental disorder
- GATM deficiency
- Gaucher disease
- Gaucher disease - ophthalmoplegia - cardiovascular calcification
- Gaucher disease collodion type
- Gaucher disease perinatal lethal
- Gaucher disease type 1
- Gaucher disease type 2
- Gaucher disease type 3
- Gaucher disease type 3C
- Gaucher disease, acute neuronopathic type
- Gaucher disease, atypical
- Gaucher disease, chronic neuronopathic type
- Gaucher disease, infantile cerebral
- Gaucher disease, juvenile and adult, cerebral
- Gaucher disease, noncerebral juvenile
- Gaucher disease, perinatal-lethal form
- Gaucher disease, subacute neuronopathic type
- Gaucher disease, type IIIC
- Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
- Gaucher ichthyosis restrictive dermopathy
- Gaucher splenomegaly
- Gaucher-like disease
- Gaucher-like disease
- GAVE
- Gay Feinmesser Cohen syndrome
- Gaze palsy
- Gaze Palsy, Familial Horizontal, With Progressive Scoliosis
- Gaze palsy, horizontal, with progressive scoliosis
- GBA DEFICIENCY
- GBBB syndrome
- GBS
- GCA
- GCBL
- GCC
- GCC of the cervix
- GCL
- GCL
- GCL4
- GCM
- GCM syndrome
- GCPS
- GCS
- GCS 1
- GCS1-CDG
- GCSE
- GCT of bone
- GCT of the ovary
- GD 1
- GD 2
- GD 3
- GDLD
- GDS
- Gelatinous ascites
- Gelatinous drop-like corneal dystrophy
- Geleophysic dwarfism
- Geleophysic dysplasia
- Gelineau syndrome
- Gelineau's syndrome
- Gemignani syndrome
- Gemistocytic astrocytoma (histologic variant)
- GEMSS
- Genee-Wiedemann acrofacial dysostosis
- Genee-Wiedemann syndrome
- Generalized arterial calcification in infancy
- Generalized atrophic benign epidermolysis bullosa
- Generalized congenital lipodystrophy
- Generalized congenital lipodystrophy with myopathy
- Generalized convulsive status epilepticus
- Generalized deciduous skin
- Generalized dominant dystrophic epidermolysis bullosa
- Generalized EBS
- Generalized elastolysis
- Generalized enamel hypoplasia and renal dysfunction
- Generalized junctional epidermolysis bullosa, non-Herlitz type
- Generalized lichenoid papular eruption
- Generalized lipodystrophy-associated progeroid syndrome
- Generalized mitis RDEB
- Generalized papular and sclerodermoid
- Generalized papular and sclerodermoid lichen myxedematosus
- Generalized peeling skin syndrome
- Generalized PHA1
- Generalized progeroid lipodystrophy due to LMNA T10I mutation
- Generalized pseudohypoaldosteronism type 1
- Generalized PSS
- Generalized pustular psoriasis
- Generalized resistance to thyroid hormone
- Genetic breast cancer- not a rare disease.
- Genetic periodic paralysis
- Genetic reflex epilepsy
- Geniculate neuralgia
- Geniospasm
- Genital anomaly with cardiomyopathy
- Genital dwarfism
- Genital dwarfism, Turner type
- Genital renal ear syndrome
- Genital retraction syndrome
- Genito palato cardiac syndrome
- Genitopalatocardiac syndrome
- Genito-palato-cardiac syndrome
- Genitopatellar syndrome
- Genoa syndrome
- Genochondromatosis
- Gentile syndrome
- Genu valgum, hereditary pubertal
- Genu valgum, st Helena familial
- Genuine diffuse phlebectasia
- Geographic choroiditis
- Geographic helicoid peripapillary choroidopathy (GHPC)
- Geographic serpiginous choroiditis
- Geographic tongue- not a rare disease.
- GEP tumors
- Gerhardt syndrome
- Germ cell tumor of testis - Another name for Testicular germ cell tumor
- Germ cells tumors
- German measles
- German type amyloidosis
- Germinal cell aplasia
- Germinoma of the central nervous system
- Geroderma osteodysplastica
- Geroderma osteodysplasticum
- Gerodermia osteodysplastica
- Gershinibaruch Leibo syndrome
- Gershoni-Baruch syndrome
- Gerstmann Badal syndrome
- Gerstmann Straussler Scheinker syndrome
- Gerstmann syndrome
- Gerstmann tetrad
- Gerstmann-Straussler-Scheinker disease
- Gerstmann-Straussler-Scheinker syndrome
- Gestagenic diabetes insipidus
- Gestational diabetes insipidus
- Gestational gigantomastia (subtype)
- Gestational pemphigoid
- Gestational trophoblastic disease
- Gestational trophoblastic neoplasm
- Gestational trophoblastic tumor
- GFD
- GFND1
- GFND2
- GGF1
- GGF2
- GGF3
- GGF4
- GGM
- GGT deficiency
- GGT1 deficiency
- GHDD
- Ghosal hematodiaphyseal dysplasia
- Ghosal hematodiaphyseal dysplasia syndrome
- Ghosal syndrome
- Ghose Sachdev Kumar syndrome
- Giaccai type acroosteolysis
- Gianotti Crosti syndrome
- Giant axonal neuropathy
- Giant axonal neuropathy 1
- Giant cell arteritis
- Giant cell chondrodysplasia
- Giant cell fibroblastoma
- Giant Cell Hepatitis (formerly)
- Giant cell inclusion disease
- Giant cell myocarditis
- Giant cell tumor of bone
- Giant condyloma acuminatum involving the prepuce and glans penis
- Giant condyloma of Buschke and Löwenstein
- Giant congenital melanocytic nevus
- Giant congenital nevus
- Giant granulocellular Abrikosov's tumor
- Giant hairy nevus
- Giant hamartoma of the breast
- Giant hypertrophic gastritis
- Giant hypertrophic gastropathy
- Giant hypertrophy of the gastric mucosa
- Giant lymph node hyperplasia
- Giant mammary hamartoma
- Giant papillary conjunctivitis
- Giant pelvic retroperitoneal liposarcoma
- Giant pigmented hairy nevus
- Giant pigmented nevus
- Giant platelet disease
- Giant platelet syndrome
- Giant tongue
- Gibraltar fever
- Giedion syndrome
- Giedion-Langer syndrome
- Gigantism
- Gigantism advanced bone age hoarse cry
- Gigantomastia
- Gilbert syndrome- not a rare disease.
- Gilbert's disease- not a rare disease.
- Gilchrist's disease
- Gilles de la Tourette's syndrome- not a rare disease.
- Gillespie syndrome
- GINGF1
- GINGF2
- GINGF3
- GINGF4
- Gingival fibromatosis with progressive deafness
- Gingival fibromatosis combined with cherubism
- Gingival fibromatosis with craniofacial dysmorphism
- Gingival fibromatosis with distinctive facies
- Gingival fibromatosis with hypertrichosis
- Gingival fibromatosis with sensorineural hearing loss
- Gingival fibromatosis, 1
- Gingival fibromatosis, 2
- Gingival fibromatosis, 3
- Gingival fibromatosis, 4
- Gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly
- Gingival hypertrophy corneal dystrophy
- Girate atrophy of the retina
- Giroux Barbeau Syndrome
- GIST
- Gitelman syndrome
- Gitelman's syndrome
- Giuffré-Tsukahara syndrome
- GJB2-related deafness
- GK deficiency
- GK1 deficiency
- GKD
- GLA deficiency
- Glanders
- Glanzmann thrombasthenia
- Glanzmann thrombasthenia type A
- Glass syndrome
- Glassy cell adenocarcinoma of the uterine cervix
- Glassy cell carcinoma of the cervix
- Glastre Cochat Bouvier syndrome
- Glaucoma 1, open angle, A
- Glaucoma 3 primary infantile B
- Glaucoma hereditary, juvenile
- Glaucoma iridogoniodysgenesia
- Glaucoma primary congenita type 3B
- Glaucoma sleep apnea
- Glaucoma type 1C
- Glaucoma, congenital
- Glaucoma, Ectopia, Microspherophakia, Stiff joints and Short stature syndrome
- Glaucoma, hereditary
- Glaucoma, hereditary adult type 1A
- Glaucoma, hereditary juvenile type 1B
- Glaucoma, primary infantile type 3A
- Glaucomatocyclitic crisis
- GLB 1 deficiency
- GLB deficiency type 1
- GLC1A
- GLC3 type B
- GLC3B
- GLD
- Gleich syndrome
- Glioblastoma
- Glioblastoma multiforme
- Glioma
- Glioma-polyposis syndrome
- Gliomatosis cerebri
- Gliomatosis peritonei
- Gliosarcoma
- Global disaccharide intolerance
- Globoid cell leukodystrophy
- Globoid cell leukoencephalopathy
- Globozoospermia
- GLOBOZOOSPERMIA, COMPLETE
- GLOBOZOOSPERMIA, TOTAL
- Glomerular basement membrane disease, nail-patella syndrome type
- Glomerular nephritis familial with fibronectin deposits
- Glomerulocystic kidney disease, hypoplastic type
- Glomerulocystic kidney, familial hypoplastic
- Glomerulonephritis
- Glomerulonephritis - mesangial proliferative
- Glomerulonephritis - pulmonary hemorrhage
- Glomerulonephritis membranoproliferative type 2
- Glomerulonephritis with sparse hair and telangiectases
- Glomerulonephritis, IGA
- Glomerulonephritis, membranous
- Glomerulopathy with fibronectin deposits 1
- Glomerulopathy with fibronectin deposits 2
- Glomerulopathy with giant fibrillar deposits
- Glomerulosclerosis, focal
- Glomus jugulare tumors
- Glomus tumor
- Glomus tumors familial 1
- Glomus tumors, familial, 2
- Glomus tumors, familial, 3
- Glomus tympanicum paraganglioma
- Glomus tympanicum tumor
- Glomus vagale tumor
- Gloomy face syndrome
- Glossodynia
- Glossopalatine ankylosis micrognathia ear anomalies
- Glossopharyngeal neuralgia
- Glossoptosis, micrognathia, and cleft palate
- Glucagonoma
- Glucagonoma syndrome
- Glucocerebrosidase deficiency
- Glucocerebrosidosis
- Glucocorticoid resistance
- Glucocorticoid sensitive hypertension
- Glucocorticoid-remediable aldosteronism
- Glucosamine N-acetyl-6-sulfatase deficiency
- Glucose galactose malabsorption deficiency
- Glucose transport defect, blood-brain barrier
- Glucose transporter protein syndrome
- Glucose transporter type 1 deficiency syndrome
- Glucose-6-phosphatase deficiency
- Glucose-6-phosphatase deficiency glycogen storage disease
- Glucose-6-phosphate dehydrogenase deficiency
- Glucose-6-phosphate translocase deficiency
- Glucose-6-phosphate transport defect
- Glucose-galactose malabsorption
- Glucosephosphate isomerase deficiency
- Glucosidase 1 deficiency
- Glucosidase acid-1,4-alpha deficiency
- Glucosyl cerebroside lipidosis
- Glucosylceramidase deficiency
- Glucosyltransferase 1 deficiency
- Glucosyltransferase 2 deficiency
- GLUT1 deficiency syndrome
- GLUT-1 deficiency syndrome
- GLUT1 DS
- GLUT2 deficiency
- Glutamate decarboxylase deficiency
- Glutamate formiminotransferase deficiency
- Glutamate-aspartate transport defect
- Glutamine deficiency, congenital
- Glutamine synthetase deficiency, congenital systemic
- Glutaric acidemia 1
- Glutaric acidemia 2
- Glutaric acidemia type 1
- Glutaric acidemia type 2
- Glutaric acidemia type 3
- Glutaric acidemia type I
- Glutaric acidemia type II
- Glutaric acidemia type III
- Glutaric aciduria 1
- Glutaric aciduria 2
- Glutaric aciduria type 3
- Glutaric aciduria type III
- Glutaryl-CoA dehydrogenase deficiency
- Glutaryl-CoA oxidase deficiency
- Glutathione synthetase deficiency
- Glutathionuria
- Gluteal muscle, absence of
- Gluten intolerance- not a rare disease.
- Gluten-induced enteropathy- not a rare disease.
- Gluten-sensitive enteropathy- not a rare disease.
- Glyceraldehyde-3-phosphate dehydrogenase deficiency
- Glyceric aciduria
- Glycerol kinase deficiency
- Glycine encephalopathy
- Glycine N-methyltransferase deficiency
- Glycine synthase deficiency
- Glycinemia, ketotic
- Glycogen branching enzyme deficiency
- Glycogen debrancher deficiency
- Glycogen storage cardiomyopathy
- Glycogen storage disease 12
- Glycogen storage disease 13
- Glycogen storage disease 1A
- Glycogen storage disease 6
- Glycogen storage disease 8
- Glycogen storage disease due to GLUT2 deficiency
- Glycogen storage disease due to phosphoglucomutase deficiency
- Glycogen storage disease limited to the heart
- Glycogen storage disease type 0, liver
- Glycogen storage disease type 0, muscle
- Glycogen storage disease type 12
- Glycogen storage disease type 13
- Glycogen storage disease type 1A
- Glycogen storage disease type 1B
- Glycogen storage disease type 2
- Glycogen storage disease type 2b (formerly)
- Glycogen storage disease type 3
- Glycogen storage disease type 4
- Glycogen storage disease type 5
- Glycogen storage disease type 6
- Glycogen storage disease type 7
- Glycogen storage disease VIII
- Glycogen storage disease X
- Glycogen storage disease XI
- Glycogen Storage Disease XI
- Glycogenosis 4
- Glycogenosis Fanconi type
- Glycogenosis type 1
- Glycogenosis type 8
- Glycogen-rich adenocarcinoma
- Glycogen-rich adenoma
- Glycolic aciduria
- Glycoprotein neuraminidase deficiency
- Glycoprotein VI deficiency
- Glycoproteinosis
- Glycosylasparaginase deficiency
- Glycosylphosphatidylinositol deficiency
- Glyoxylate reductase/hydroxypyruvate reductase deficiency
- GM1 gangliosidosis
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM2 gangliosidosis, 0 variant
- GM2 gangliosidosis, type 1
- GM2 gangliosidosis, type 2
- GM2-gangliosidosis, B, B1, AB variant
- GM3 synthase deficiency
- GMPPA-CDG
- GMS syndrome
- GNAO1 encephalopathy
- Gnathodiaphyseal dysplasia
- Gnathostoma Infection
- Gnathostomiasis
- GNB4-related intermediate Charcot-Marie-Tooth neuropathy
- GNE myopathy
- GNMT deficiency
- GNPTA
- GNS deficiency
- GO
- Goblet cell adenocarcinoid
- Goblet cell carcinoid
- Goblet cell carcinoma
- Goblet cell tumor
- Goeminne syndrome
- Goiter-deafness syndrome
- Golabi-Rosen syndrome
- Goldberg syndrome
- Goldberg-Shprintzen megacolon syndrome
- Goldberg-Shprintzen syndrome
- Goldblatt chondrodysplasia
- Goldblatt syndrome
- Goldblatt Wallis syndrome
- Goldblatt-Viljoen syndrome
- Goldenhar disease
- Goldenhar syndrome
- Goldenhar syndrome with ipsilateral radial defect
- Goldmann-Favre syndrome
- Goldston syndrome
- Gollop Coates syndrome
- Gollop-Wolfgang complex
- Goltz Gorlin Syndrome
- Goltz Syndrome
- Goltz-Gorlin syndrome
- GOMBO syndrome
- Gomez Lopez Hernandez syndrome
- Gomez-Lopez-Hernández syndrome
- Gomm Button disease
- Gonadal dysgenesis
- Gonadal Dysgenesis (45,X)
- Gonadal dysgenesis mixed
- Gonadal dysgenesis Turner type
- Gonadal dysgenesis XY type associated anomalies
- Gonadal dysgenesis, XX type
- Gonadal dysgenesis, XX type, with deafness
- Gonadal dysgenesis, XY female type
- Gonadal polyembryoma
- Gonadotropin deficiency familial idiopathic
- Goniodysgenesis hypodontia
- Goniodysgenesis-intellectual disability-short stature syndrome
- Gonococcal conjunctivitis
- Gonococcal perihepatitis
- Gonzales-del Angel syndrome
- Good syndrome
- Goodpasture syndrome
- Gordon hyperkalemia-hypertension syndrome
- Gordon syndrome
- Gordon-Holmes syndrome
- Gorham's disease
- Gorham-Stout disease
- Gorham-Stout syndrome
- Gorlin Chaudhry Moss syndrome
- Gorlin syndrome
- Gorlin-Chaudhry-Moss syndrome
- Gorlin-Goltz Syndrome
- GOSHS
- GOSR2-related progressive myoclonus ataxia
- Gottron syndrome
- GP VI deficiency
- GPA
- GPAPP deficiency
- GPC
- GPHN
- GPI deficiency
- GPP
- GPS
- Gracile bone dysplasia
- GRACILE syndrome
- Grade III astrocytoma
- Graefe-Usher syndrome
- Graham Boyle Troxell syndrome
- Graham Little syndrome
- Graham Little-Piccardi-Lassueur syndrome
- Graham-Cox syndrome
- Graham-Little-Piccardi-Lassueur syndrome
- Grand Kaine Fulling syndrome
- Grant syndrome
- Granular and lattice corneal dystrophies
- Granular cell tumor
- Granular corneal dystrophy type 2
- Granular-lattice (Avellino) corneal dystrophy
- Granulocytic sarcoma
- Granulocytopenia
- Granuloma annulare
- Granuloma fungoides
- Granuloma Inguinale
- Granulomas, congenital cerebral
- Granulomatosis with polyangiitis
- Granulomatosis, familial juvenile systemic
- Granulomatosis, familial, Blau type
- Granulomatous allergic angiitis
- Granulomatous Amebic Encephalitis
- Granulomatous angiitis of the central nervous system
- Granulomatous colitis- not a rare disease.
- Granulomatous disease, chronic
- Granulomatous enteritis- not a rare disease.
- Granulomatous hypophysitis
- Granulomatous inflammatory arthritis, dermatitis, and uveitis, familial
- Granulomatous lobular mastitis
- Granulomatous rosacea
- Granulomatous slack skin
- Granulomatous slack skin disease
- Granulosa cell tumor of the ovary
- Granulosa theca cell tumor
- Granulosa theca cell tumor of the ovary
- Graphite Pneumoconiosis
- Gräsbeck-Imerslund disease
- Graves disease- not a rare disease.
- Graves' hyperthyroidism- not a rare disease.
- Gravidic intrahepatic cholestasis
- Gray platelet syndrome
- Gray zone lymphoma
- Grebe chondrodysplasia
- Grebe dysplasia
- Grebe syndrome
- Green Sandford Davison syndrome
- Greenberg dysplasia
- Greenberg skeletal dysplasia
- Greig cephalopolysyndactyly syndrome
- Greig syndrome
- Greither disease
- Greither's disease
- GRIN1-associated disorders
- GRIN2B encephalopathy
- GRIN2B related syndrome
- GRIN2B-related intellectual disability
- Griscelli disease
- Griscelli syndrome
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Griscelli syndrome with hemophagocytic syndrome
- Griscelli syndrome with neurologic impairment
- Griscelli syndrome, cutaneous and neurologic type
- Griscelli-Pruniéras syndrome type 2
- Grix Blankenship Peterson syndrome
- Groenouw type I corneal dystrophy
- Groenouw type II corneal dystrophy
- Groll Hirschowitz syndrome
- Gronblad Strandberg syndrome
- Ground itch
- Group A Streptococcal disease
- Group A Streptococcal infection
- Group B strep disease in newborns
- Grover disease- not a rare disease.
- Grover's disease- not a rare disease.
- Growth deficiency, facial anomalies, and brachydactyly
- Growth deficiency, sun-sensitive, telangiectatic, hypo and hyperpigmented skin, predisposition to malignancy and chromosomal instability
- Growth delay - intellectual disability - mandibulofacial dysostosis - microcephaly - cleft palate
- Growth delay-intellectual disability-mandibulofacial dysostosis-microcephaly-cleft palate syndrome
- GROWTH FACTORS, COMBINED DEFECT OF - Another name for Lipodystrophy due to peptidic growth factors deficiency
- Growth hormone deficiency
- Growth hormone deficiency with hypogammaglobulinemia
- Growth hormone deficiency, isolated autosomal dominant
- Growth hormone deficiency, isolated autosomal recessive
- Growth hormone excess
- Growth hormone insensitivity due to postreceptor defect
- Growth hormone insensitivity syndrome
- Growth hormone insensitivity with immunodeficiency
- Growth hormone receptor deficiency
- Growth mental deficiency syndrome of Myhre
- Growth retardation hydrocephaly lung hypoplasia
- Growth retardation prenatal with progressive pancytopenia and cerebellar hypoplasia
- Growth retardation with sensorineural deafness and mental retardation
- Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy
- Growth Retardation, Aminoaciduria, Cholestasis, Iron overload, Lactic acidosis and Early death
- Growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction
- Growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia
- Growth retardation, pulmonary hypertension, and aminoaciduria
- Growth retardation, severe mental retardation, acral limb deficiencies with poorly keratinized nails
- Growth retardation, small and puffy hands and feet, and eczema
- Growth retardation, truncal obesity, facial asymmetry, hypotonia, small phallus, malformed low-set ears and micrognathia
- GRTH
- Grubben de Cock Borghgraef syndrome
- Gruber syndrome
- GS
- GS1
- GS2
- GS3
- GSD 4
- GSD 5
- GSD II
- GSD IV
- GSD type 14
- GSD1
- GSD10
- GSD12
- GSD13
- GSD1B
- GSD2B (formerly)
- GSD6
- GSD7
- GSDX
- GSDXIV
- GSL
- GSM 1
- GSSD
- GT
- GTCT
- GTG deficiency
- GTN
- GTP cyclohydrolase I deficiency
- GTPTS
- Guadalajara camptodactyly syndrome type II
- Guam disease
- Guanidinoacetate methyltransferase deficiency
- Guerin-Stern syndrome
- Guérin-Stern syndrome
- Guibaud Vainsel syndrome
- Guillain-Barre syndrome
- Guillain-Barré syndrome
- Guillain-Barré-Strohl syndrome
- Guinea worm disease
- Guinea worm infection
- Guizar Vasquez Sanchez Manzano syndrome
- Guízar Vázquez-Sánchez-Manzano syndrome
- Gunal Seber Basaran syndrome
- Günther disease
- Gurrieri syndrome
- Gurrieri-Sammito-Bellussi syndrome
- GUSB deficiency
- Gusher syndrome
- GUST
- Gustatory sweating
- Gustavson syndrome
- Guttate hypopigmentation
- Guttate psoriasis
- Guttmacher syndrome
- GWAFD
- GWC
- GWD
- Gynandroblastoma
- Gyrate atrophy
- Gyrate atrophy of choroid and retina
NIH genetic and rare disease info[edit source]
List of rare diseases-G is a rare disease.
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD