List of rare diseases-G
From WikiMD's Food, Medicine & Wellnesspedia
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.
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