List of rare diseases-G

NIH genetic and rare disease info

• NIH info on List of rare diseases-G

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

• NIH info on List of rare diseases-G

List of rare diseases-G is a rare disease.