- 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 - See Posner-Schlossman syndrome
- GLB 1 deficiency - See GM1 gangliosidosis
- GLB deficiency type 1 - See GM1 gangliosidosis type 1
- GLC1A - See Primary open angle glaucoma juvenile onset 1
- GLC3 type B - See Glaucoma 3 primary infantile B
- GLC3B - See Glaucoma 3 primary infantile B
- GLD - See Krabbe disease
- Gleich syndrome - See Episodic angioedema with eosinophilia
- Glioblastoma
- Glioblastoma multiforme - See Glioblastoma
- Glioma
- Glioma-polyposis syndrome - See Turcot syndrome
- Gliomatosis cerebri
- Gliomatosis peritonei
- Gliosarcoma
- Global disaccharide intolerance
- Globoid cell leukodystrophy - See Krabbe disease
- Globoid cell leukoencephalopathy - See Krabbe disease
- Globozoospermia
- GLOBOZOOSPERMIA, COMPLETE - See Globozoospermia
- GLOBOZOOSPERMIA, TOTAL - See Globozoospermia
- Glomerular basement membrane disease, nail-patella syndrome type - See Salcedo syndrome
- Glomerular nephritis familial with fibronectin deposits - See Glomerulopathy with fibronectin deposits 2
- Glomerulocystic kidney disease, hypoplastic type - See Maturity-onset diabetes of the young
- Glomerulocystic kidney, familial hypoplastic - See Maturity-onset diabetes of the young
- Glomerulonephritis
- Glomerulonephritis - mesangial proliferative - See Mesangial proliferative glomerulonephritis
- Glomerulonephritis - pulmonary hemorrhage - See Goodpasture syndrome
- Glomerulonephritis membranoproliferative type 2 - See Dense deposit disease
- Glomerulonephritis with sparse hair and telangiectases
- Glomerulonephritis, IGA - See IgA nephropathy
- Glomerulonephritis, membranous - See Membranous nephropathy
- Glomerulopathy with fibronectin deposits 1
- Glomerulopathy with fibronectin deposits 2
- Glomerulopathy with giant fibrillar deposits - See Glomerulopathy with fibronectin deposits 1
- Glomerulosclerosis, focal - See Focal segmental glomerulosclerosis
- Glomus jugulare tumors
- Glomus tumor - See Glomus jugulare tumors
- Glomus tumors familial 1 - See Paragangliomas 1
- Glomus tumors, familial, 2 - See Paragangliomas 2
- Glomus tumors, familial, 3 - See Paragangliomas 3
- Glomus tympanicum paraganglioma - See Glomus tympanicum tumor
- Glomus tympanicum tumor
- Glomus vagale tumor
- Gloomy face syndrome - See 3M syndrome
- Glossodynia
- Glossopalatine ankylosis cataracts digital anomalies - See Johnson Hall Krous syndrome
- Glossopalatine ankylosis micrognathia ear anomalies
- Glossopharyngeal neuralgia
- Glossoptosis, micrognathia, and cleft palate - See Pierre Robin sequence
- Glucagonoma
- Glucagonoma syndrome
- Glucocerebrosidase deficiency - See Gaucher disease type 1
- Glucocerebrosidosis - See Gaucher disease
- Glucocorticoid resistance
- Glucocorticoid sensitive hypertension - See Glucocorticoid-remediable aldosteronism
- Glucocorticoid-remediable aldosteronism
- Glucosamine N-acetyl-6-sulfatase deficiency - See Mucopolysaccharidosis type IIID
- Glucose galactose malabsorption deficiency - See Glucose-galactose malabsorption
- Glucose transport defect, blood-brain barrier - See Glucose transporter type 1 deficiency syndrome
- Glucose transporter protein syndrome - See Glucose transporter type 1 deficiency syndrome
- Glucose transporter type 1 deficiency syndrome
- Glucose-6-phosphatase deficiency - See Glycogen storage disease type 1A
- Glucose-6-phosphatase deficiency glycogen storage disease - See Glycogen storage disease type 1A
- Glucose-6-phosphate dehydrogenase deficiency
- Glucose-6-phosphate translocase deficiency
- Glucose-6-phosphate transport defect - See Glycogen storage disease type 1B
- Glucose-galactose malabsorption
- Glucosephosphate isomerase deficiency
- Glucosidase 1 deficiency - See MOGS-CDG (CDG-IIb)
- Glucosidase acid-1,4-alpha deficiency
- Glucosyl cerebroside lipidosis - See Gaucher disease
- Glucosylceramidase deficiency - See Gaucher disease
- Glucosyltransferase 1 deficiency - See ALG6-CDG (CDG-Ic)
- Glucosyltransferase 2 deficiency - See ALG8-CDG (CDG-Ih)
- GLUT1 deficiency syndrome - See Glucose transporter type 1 deficiency syndrome
- GLUT-1 deficiency syndrome - See Glucose transporter type 1 deficiency syndrome
- GLUT1 DS - See Glucose transporter type 1 deficiency syndrome
- GLUT2 deficiency - See Fanconi Bickel syndrome
- Glutamate decarboxylase deficiency
- Glutamate formiminotransferase deficiency
- Glutamate-aspartate transport defect - See Dicarboxylic aminoaciduria
- Glutamine deficiency, congenital
- Glutamine synthetase deficiency, congenital systemic - See Glutamine deficiency, congenital
- Glutaric acidemia 1 - See Glutaric acidemia type I
- Glutaric acidemia 2 - See Glutaric acidemia type II
- Glutaric acidemia type 1 - See Glutaric acidemia type I
- Glutaric acidemia type 2 - See Glutaric acidemia type II
- Glutaric acidemia type 3 - See Glutaric acidemia type III
- Glutaric acidemia type I
- Glutaric acidemia type II
- Glutaric acidemia type III
- Glutaric aciduria 1 - See Glutaric acidemia type I
- Glutaric aciduria 2 - See Glutaric acidemia type II
- Glutaric aciduria type 3 - See Glutaric acidemia type III
- Glutaric aciduria type III - See Glutaric acidemia type III
- Glutaryl-CoA dehydrogenase deficiency - See Glutaric acidemia type I
- Glutaryl-CoA oxidase deficiency - See Glutaric acidemia type III
- Glutathione synthetase deficiency
- Glutathionuria
- Gluteal muscle, absence of - See Absence of gluteal muscle
- Gluten intolerance - See Celiac disease - not a rare disease
- Gluten-induced enteropathy - See Celiac disease - not a rare disease
- Gluten-sensitive enteropathy - See Celiac disease - not a rare disease
- Glyceraldehyde-3-phosphate dehydrogenase deficiency
- Glyceric aciduria - See Primary hyperoxaluria type 2
- Glycerol kinase deficiency - See Hyperglycerolemia
- Glycine encephalopathy
- Glycine N-methyltransferase deficiency
- Glycine synthase deficiency - See Glycine encephalopathy
- Glycinemia, ketotic - See Propionic acidemia
- Glycogen branching enzyme deficiency - See Glycogen storage disease type 4
- Glycogen debrancher deficiency - See Glycogen storage disease type 3
- Glycogen storage cardiomyopathy - See Danon disease
- Glycogen storage disease 12 - See Glycogen storage disease type 12
- Glycogen storage disease 13 - See Glycogen storage disease type 13
- Glycogen storage disease 1A - See Glycogen storage disease type 1A
- Glycogen storage disease 6 - See Glycogen storage disease type 6
- Glycogen storage disease 8
- Glycogen storage disease due to GLUT2 deficiency - See Fanconi Bickel syndrome
- Glycogen storage disease due to phosphoglucomutase deficiency - See PGM1-CDG
- Glycogen storage disease limited to the heart - See Danon disease
- 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) - See Danon disease
- 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 - See Glycogen storage disease 8
- Glycogen storage disease X - See Phosphoglycerate mutase deficiency
- Glycogen storage disease XI - See Fanconi Bickel syndrome
- Glycogen Storage Disease XI - See Lactate dehydrogenase A deficiency
- Glycogenosis 4 - See Glycogen storage disease type 4
- Glycogenosis Fanconi type - See Fanconi Bickel syndrome
- Glycogenosis type 1 - See Glycogen storage disease type 1A
- Glycogenosis type 8 - See Glycogen storage disease 8
- Glycogen-rich adenocarcinoma - See Epithelial-myoepithelial carcinoma
- Glycogen-rich adenoma - See Epithelial-myoepithelial carcinoma
- Glycolic aciduria - See Primary hyperoxaluria type 1
- Glycoprotein neuraminidase deficiency - See Sialidosis, type II
- Glycoprotein VI deficiency
- Glycoproteinosis
- Glycosylasparaginase deficiency - See Aspartylglycosaminuria
- Glycosylphosphatidylinositol deficiency - See Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- Glyoxylate reductase/hydroxypyruvate reductase deficiency - See Primary hyperoxaluria type 2
- GM1 gangliosidosis
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM2 gangliosidosis, 0 variant
- GM2 gangliosidosis, type 1 - See Tay-Sachs disease
- GM2 gangliosidosis, type 2 - See Sandhoff disease
- GM2-gangliosidosis, B, B1, AB variant
- GM3 synthase deficiency
- GMPPA-CDG
- GMS syndrome
- GNAO1 encephalopathy
- Gnathodiaphyseal dysplasia - See Osteogenesis imperfecta Levin type
- Gnathostoma Infection
- Gnathostomiasis - See Gnathostoma Infection
- GNB4-related intermediate Charcot-Marie-Tooth neuropathy - See Autosomal dominant intermediate Charcot-Marie-Tooth
- GNE myopathy - See Inclusion body myopathy 2
- GNMT deficiency - See Glycine N-methyltransferase deficiency
- GNPTA - See I cell disease
- GNS deficiency - See Mucopolysaccharidosis type IIID
- GO - See Geroderma osteodysplastica
- Goblet cell adenocarcinoid - See Goblet cell carcinoid
- Goblet cell carcinoid
- Goblet cell carcinoma - See Goblet cell carcinoid
- Goblet cell tumor - See Goblet cell carcinoid
- Goeminne syndrome - See Torticollis keloids cryptorchidism renal dysplasia
- Goiter-deafness syndrome - See Pendred syndrome
- Golabi-Rosen syndrome - See Simpson-Golabi-Behmel syndrome
- Goldberg syndrome - See Galactosialidosis
- Goldberg-Shprintzen megacolon syndrome
- Goldberg-Shprintzen syndrome - See Goldberg-Shprintzen megacolon syndrome
- Goldblatt chondrodysplasia - See Spondylometaphyseal dysplasia with dentinogenesis imperfecta
- Goldblatt syndrome - See Spondylometaphyseal dysplasia with dentinogenesis imperfecta
- Goldblatt Wallis syndrome - See Hypospadias-intellectual disability, Goldblatt type syndrome
- Goldblatt-Viljoen syndrome - See Radial ray hypoplasia choanal atresia
- Goldenhar disease
- Goldenhar syndrome - See Goldenhar disease
- Goldenhar syndrome with ipsilateral radial defect - See Microsomia hemifacial radial defects
- Goldmann-Favre syndrome
- Goldston syndrome - See Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia
- Gollop Coates syndrome
- Gollop-Wolfgang complex - See Femur bifid with monodactylous ectrodactyly
- Goltz Gorlin Syndrome - See Focal dermal hypoplasia
- Goltz Syndrome - See Focal dermal hypoplasia
- Goltz-Gorlin syndrome - See Focal dermal hypoplasia
- GOMBO syndrome
- Gomez Lopez Hernandez syndrome
- Gomez-Lopez-Hernández syndrome - See Gomez Lopez Hernandez syndrome
- Gomm Button disease - See Acute febrile neutrophilic dermatosis
- Gonadal dysgenesis
- Gonadal Dysgenesis (45,X) - See Turner syndrome
- Gonadal dysgenesis mixed
- Gonadal dysgenesis Turner type
- Gonadal dysgenesis XY type associated anomalies
- Gonadal dysgenesis, XX type - See Perrault syndrome
- Gonadal dysgenesis, XX type, with deafness - See Perrault syndrome
- Gonadal dysgenesis, XY female type - See Swyer syndrome
- Gonadal polyembryoma - See Polyembryoma
- Gonadotropin deficiency familial idiopathic - See Eunuchoidism familial hypogonadotropic
- Goniodysgenesis hypodontia - See Axenfeld-Rieger syndrome
- Goniodysgenesis-intellectual disability-short stature syndrome - See GMS syndrome
- Gonococcal conjunctivitis
- Gonococcal perihepatitis - See Fitz-Hugh-Curtis syndrome
- Gonzales-del Angel syndrome - See Delayed membranous cranial ossification
- Good syndrome - See Immunodeficiency with thymoma
- Goodpasture syndrome
- Gordon hyperkalemia-hypertension syndrome - See Pseudohypoaldosteronism type 2
- Gordon syndrome
- Gordon-Holmes syndrome - See Cerebellar ataxia and hypogonadotropic hypogonadism
- Gorham's disease
- Gorham-Stout disease - See Gorham's disease
- Gorham-Stout syndrome - See Gorham's disease
- Gorlin Bushkell Jensen syndrome
- Gorlin Chaudhry Moss syndrome
- Gorlin syndrome - See Nevoid basal cell carcinoma syndrome
- Gorlin-Chaudhry-Moss syndrome - See Gorlin Chaudhry Moss syndrome
- Gorlin-Goltz Syndrome - See Nevoid basal cell carcinoma syndrome
- GOSHS - See Goldberg-Shprintzen megacolon syndrome
- GOSR2-related progressive myoclonus ataxia
- Gottron syndrome - See Acrogeria, Gottron type
- GP VI deficiency - See Glycoprotein VI deficiency
- GPA - See Granulomatosis with polyangiitis
- GPAPP deficiency - See Chondrodysplasia with joint dislocations, GPAPP type
- GPC - See Giant papillary conjunctivitis
- GPHN - See Giant congenital nevus
- GPI deficiency - See Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- GPP - See Generalized pustular psoriasis
- GPS - See Gray platelet syndrome
- Gracile bone dysplasia
- GRACILE syndrome
- Grade III astrocytoma - See Anaplastic astrocytoma
- Graefe-Usher syndrome - See Usher syndrome
- Graham Boyle Troxell syndrome
- Graham Little syndrome - See Graham-Little-Piccardi-Lassueur syndrome
- Graham Little-Piccardi-Lassueur syndrome - See Graham-Little-Piccardi-Lassueur syndrome
- Graham-Cox syndrome
- Graham-Little-Piccardi-Lassueur syndrome
- Grand Kaine Fulling syndrome
- Grant syndrome
- Granular and lattice corneal dystrophies - See Corneal dystrophy Avellino type
- Granular cell tumor
- Granular corneal dystrophy type 2 - See Corneal dystrophy Avellino type
- Granular-lattice (Avellino) corneal dystrophy - See Corneal dystrophy Avellino type
- Granulocytic sarcoma - See Myeloid sarcoma
- Granulocytopenia
- Granuloma annulare
- Granuloma fungoides - See Mycosis fungoides
- Granuloma Inguinale
- Granulomas, congenital cerebral
- Granulomatosis with polyangiitis
- Granulomatosis, familial juvenile systemic - See Blau syndrome
- Granulomatosis, familial, Blau type - See Blau syndrome
- Granulomatous allergic angiitis - See Eosinophilic granulomatosis with polyangiitis
- Granulomatous Amebic Encephalitis
- Granulomatous angiitis of the central nervous system - See Primary angiitis of the central nervous system
- Granulomatous colitis - See Crohn's disease - not a rare disease
- Granulomatous disease, chronic - See Chronic granulomatous disease
- Granulomatous enteritis - See Crohn's disease - not a rare disease
- Granulomatous hypophysitis
- Granulomatous inflammatory arthritis, dermatitis, and uveitis, familial - See Blau syndrome
- Granulomatous lobular mastitis
- Granulomatous rosacea
- Granulomatous slack skin - See Granulomatous slack skin disease
- Granulomatous slack skin disease
- Granulosa cell tumor of the ovary
- Granulosa theca cell tumor - See Granulosa cell tumor of the ovary
- Granulosa theca cell tumor of the ovary - See Granulosa cell tumor of the ovary
- Graphite Pneumoconiosis
- Gräsbeck-Imerslund disease - See Imerslund-Grasbeck syndrome
- Graves' disease
- Graves' hyperthyroidism - See Graves' disease
- Gravidic intrahepatic cholestasis - See Intrahepatic cholestasis of pregnancy
- Gray platelet syndrome
- Gray zone lymphoma
- Grebe chondrodysplasia - See Chondrodysplasia, Grebe type
- Grebe dysplasia - See Chondrodysplasia, Grebe type
- Grebe syndrome - See Chondrodysplasia, Grebe type
- Green Sandford Davison syndrome
- Greenberg dysplasia
- Greenberg skeletal dysplasia - See Greenberg dysplasia
- Greig cephalopolysyndactyly syndrome
- Greig syndrome - See Greig cephalopolysyndactyly syndrome
- Greither disease - See Keratoderma palmoplantaris transgrediens
- Greither's disease - See Keratoderma palmoplantaris transgrediens
- GRIN1-associated disorders
- GRIN2B encephalopathy - See GRIN2B related syndrome
- GRIN2B related syndrome
- GRIN2B-related intellectual disability - See GRIN2B related syndrome
- Griscelli disease - See Griscelli syndrome
- Griscelli syndrome
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Griscelli syndrome with hemophagocytic syndrome - See Griscelli syndrome type 2
- Griscelli syndrome with neurologic impairment - See Griscelli syndrome type 1
- Griscelli syndrome, cutaneous and neurologic type - See Griscelli syndrome type 1
- Griscelli-Pruniéras syndrome type 2 - See Griscelli syndrome type 2
- Grix Blankenship Peterson syndrome
- Groenouw type I corneal dystrophy
- Groenouw type II corneal dystrophy - See Macular dystrophy, corneal type 1
- Groll Hirschowitz syndrome
- Gronblad Strandberg syndrome - See Pseudoxanthoma elasticum
- Ground itch - See Cutaneous larva migrans
- Group A Streptococcal disease - See Streptococcal Group A invasive disease
- Group A Streptococcal infection - See Streptococcal Group A invasive disease
- Group B strep disease in newborns
- Grover disease - See Grover's disease - not a rare disease
- Grover's disease - not a rare disease
- Growth deficiency, facial anomalies, and brachydactyly - See Frias syndrome
- Growth deficiency, sun-sensitive, telangiectatic, hypo and hyperpigmented skin, predisposition to malignancy and chromosomal instability - See Bloom syndrome
- Growth delay - intellectual disability - mandibulofacial dysostosis - microcephaly - cleft palate - See Mandibulofacial dysostosis with microcephaly
- Growth delay-intellectual disability-mandibulofacial dysostosis-microcephaly-cleft palate syndrome - SeeMandibulofacial dysostosis with microcephaly
- GROWTH FACTORS, COMBINED DEFECT OF - Another name for Lipodystrophy due to peptidic growth factors deficiency
- Growth hormone deficiency
- Growth hormone deficiency with hypogammaglobulinemia - See Isolated growth hormone deficiency type 3
- Growth hormone deficiency, isolated autosomal dominant - See Isolated growth hormone deficiency type 2
- Growth hormone deficiency, isolated autosomal recessive - See Isolated growth hormone deficiency type 1A
- Growth hormone excess - See Acromegaly
- Growth hormone insensitivity due to postreceptor defect - See Growth hormone insensitivity with immunodeficiency
- Growth hormone insensitivity syndrome - See Laron syndrome
- Growth hormone insensitivity with immunodeficiency
- Growth hormone receptor deficiency - See Laron syndrome
- Growth mental deficiency syndrome of Myhre - See Myhre syndrome
- Growth retardation alopecia pseudoanodontia optic
- Growth retardation hydrocephaly lung hypoplasia
- Growth retardation prenatal with progressive pancytopenia and cerebellar hypoplasia - See Hoyeraal Hreidarsson syndrome
- Growth retardation with sensorineural deafness and mental retardation - See Insulin-like growth factor I deficiency
- Growth retardation, Alopecia, Pseudoanodontia and Optic atrophy - See GAPO syndrome
- Growth Retardation, Aminoaciduria, Cholestasis, Iron overload, Lactic acidosis and Early death - See GRACILE syndrome
- Growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction - See Deafness, epiphyseal dysplasia, short stature
- Growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia - See GOMBO syndrome
- Growth retardation, pulmonary hypertension, and aminoaciduria - See Rowley-Rosenberg syndrome
- Growth retardation, severe mental retardation, acral limb deficiencies with poorly keratinized nails - See Cartwright Nelson Fryns syndrome
- Growth retardation, small and puffy hands and feet, and eczema - See Grubben de Cock Borghgraef syndrome
- Growth retardation, truncal obesity, facial asymmetry, hypotonia, small phallus, malformed low-set ears and micrognathia - See Diploid-triploid mosaicism
- GRTH - See Generalized resistance to thyroid hormone
- Grubben de Cock Borghgraef syndrome
- Gruber syndrome - See Meckel syndrome
- GS - See Gerstmann syndrome
- GS1 - See Griscelli syndrome type 1
- GS2 - See Griscelli syndrome type 2
- GS3 - See Griscelli syndrome type 3
- GSD 4 - See Glycogen storage disease type 4
- GSD 5 - See Glycogen storage disease type 5
- GSD II - See Glycogen storage disease type 2
- GSD IV - See Glycogen storage disease type 4
- GSD type 14 - See PGM1-CDG
- GSD1 - See Glycogen storage disease type 1A
- GSD10 - See Phosphoglycerate mutase deficiency
- GSD12 - See Glycogen storage disease type 12
- GSD13 - See Glycogen storage disease type 13
- GSD1B - See Glycogen storage disease type 1B
- GSD2B (formerly) - See Danon disease
- GSD6 - See Glycogen storage disease type 6
- GSD7 - See Glycogen storage disease type 7
- GSDX - See Phosphoglycerate mutase deficiency
- GSDXIV - See PGM1-CDG
- GSL - See Galactosialidosis
- GSM 1 - See Hereditary geniospasm
- GSSD - See Gerstmann-Straussler-Scheinker disease
- GT - See Glanzmann thrombasthenia
- GTCT - See Granulosa cell tumor of the ovary
- GTG deficiency - See Glutathionuria
- GTN - See Gestational trophoblastic tumor
- GTP cyclohydrolase I deficiency
- GTPTS - See Genitopatellar syndrome
- Guadalajara camptodactyly syndrome type II - See Camptodactyly syndrome Guadalajara type 2
- Guam disease - See Amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
- Guanidinoacetate methyltransferase deficiency
- Guerin-Stern syndrome - See Arthrogryposis multiplex congenita
- Guérin-Stern syndrome - See Arthrogryposis multiplex congenita
- Guibaud Vainsel syndrome - See Osteopetrosis autosomal recessive 3
- Guillain-Barre syndrome
- Guillain-Barré syndrome - See Guillain-Barre syndrome
- Guillain-Barré-Strohl syndrome - See Guillain-Barre syndrome
- Guinea worm disease - See Dracunculiasis
- Guinea worm infection - See Dracunculiasis
- Guizar Vasquez Sanchez Manzano syndrome
- Guízar Vázquez-Sánchez-Manzano syndrome - See Guizar Vasquez Sanchez Manzano syndrome
- Gunal Seber Basaran syndrome - See Osteopoikilosis and dacryocystitis
- Günther disease - See Congenital erythropoietic porphyria
- Gupta Patton syndrome
- Gurrieri syndrome
- Gurrieri-Sammito-Bellussi syndrome - See Gurrieri syndrome
- GUSB deficiency - See Mucopolysaccharidosis type VII
- Gusher syndrome - See Deafness, X-linked 2
- GUST - See Severe X-linked intellectual disability, Gustavson type
- Gustatory sweating - See Frey's syndrome
- Gustavson syndrome - See Severe X-linked intellectual disability, Gustavson type
- Guttate hypopigmentation - See Cole disease
- Guttate psoriasis
- Guttmacher syndrome - See Preaxial deficiency, postaxial polydactyly and hypospadias
- GWAFD - See Miller syndrome
- GWC - See Femur bifid with monodactylous ectrodactyly
- GWD - See Dracunculiasis
- Gynandroblastoma
- Gyrate atrophy - See Gyrate atrophy of choroid and retina
- Gyrate atrophy of choroid and retina
sábado, 26 de enero de 2019
Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
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