G

G6P deficiency
G6P deficiency type 1a
G6P deficiency type Ib
G6PT deficiency
G6P translocase deficiency
GA1
GABA transaminase deficiency
GABEB
Gabriele-de Vries syndrome
Gaisböck syndrome
Galactocerebrosidase deficiency
Galactokinase deficiency
Galactokinase deficiency galactosemia
Galactosamine-6-sulfatase deficiency
Galactose-1-phosphate uridyltransferase deficiency
Galactose epimerase deficiency
Galactosemia
Galactosemia type 1
Galactosemia type 2
Galactosemia type 3
Galactosialidosis
Galactosylceramidase deficiency
GALC deficiency
GALE-D
GALE deficiency
GALK-D
GALK deficiency
Gallbladder neuroendocrine tumor
Galloway-Mowat syndrome
Galloway syndrome
GALNS deficiency
GALT deficiency
Gamborg-Nielsen syndrome
Game-Friedman-Paradice syndrome
Gamma-aminobutyric acid transaminase deficiency
Gamma-cystathionase deficiency
Gamma-glutamylcysteine synthetase deficiency
Gamma-glutamyl transferase deficiency
Gamma-glutamyl transpeptidase deficiency
Gamma-HCD
Gamma-heavy chain disease
Gamma-hydroxybutyric aciduria
Gamma-sarcoglycanopathy
Gamstorp disease
Gamstorp episodic adynamy
GAMT deficiency
GAN
Gangliocytoma
Ganglioglioma
Ganglioneuroblastoma
Ganglioneuroma
Gangliosidosis
GAPO syndrome
GAPPS
Garcia-Lurie syndrome
Gardner-Diamond syndrome
Gardner-Silengo-Wachtel syndrome
Gardner syndrome
Gass disease
Gastric adenocarcinoma and proximal polyposis of the stomach
Gastric duplication cyst of the tongue
Gastric intrinsic factor deficiency
Gastric linitis plastica
Gastric NET
Gastric neuroendocrine tumor
Gastric squamous cell carcinoma
Gastrinoma
Gastrocutaneous syndrome
Gastroduodenal malformation
Gastroenteric neuroendocrine neoplasm
Gastroenteropancreatic neuroendocrine neoplasm
Gastrointestinal polyposis-ectodermal changes syndrome
Gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome
Gastrointestinal stromal sarcoma
Gastrointestinal stromal tumor
Gastroschisis
Gaucher disease
Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
Gaucher disease, subacute neuronopathic type
Gaucher disease type 1
Gaucher disease type 2
Gaucher disease type 3
Gaucher disease type 3C
Gaucher-like disease
GBE deficiency, adult neuromuscular form
GBE deficiency, childhood combined hepatic and myopathic form
GBE deficiency, childhood neuromuscular form
GBE deficiency, congenital neuromuscular form
GBE deficiency, fatal perinatal neuromuscular form
GBE deficiency, non progressive hepatic form
GBE deficiency, progressive hepatic form
GBM
GBS
GBS, acute inflammatory demyelinating polyradiculoneuropathic form
GCC
GCD1
GCD2
GCDHD
GCDI
GCDII
GCGR-related hyperglucagonemia
GCL
GCM syndrome
GCPS
GCT of bone
GDCD
GDD
GDE deficiency
GDS
GEFS+
GEKA
Gelatinous ascites
Gelatinous drop-like corneal dystrophy
Geleophysic dwarfism
Geleophysic dysplasia
Gélineau disease
Gelsolin amyloidosis
Gemignani syndrome
Gemistocytic astrocytoma
GEMSS syndrome
Generalized arterial calcification of infancy
Generalized atrophic benign epidermolysis bullosa
Generalized basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss
Generalized basaloid follicular hamartoma syndrome
Generalized bulbospinal muscular atrophy
Generalized cervical and upper-limb-onset dystonia
Generalized congenital lipodystrophy
Generalized deciduous skin
Generalized deciduous skin type A
Generalized deciduous skin type B
Generalized deciduous skin type C
Generalized dominant dystrophic epidermolysis bullosa
Generalized EBS, non-Dowling-Meara type
Generalized enchondromatosis with platyspondyly
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Generalized epilepsy-paroxysmal dyskinesia syndrome
Generalized epilepsy with febrile seizures-plus
Generalized epimerase deficiency galactosemia
Generalized eruptive histiocytoma
Generalized eruptive histiocytosis
Generalized eruptive keratoacanthoma
Generalized eruptive keratoacanthomas of Grzybowski
Generalized essential telangiectasia
Generalized exfoliative disease
Generalized fetal edema
Generalized galactose epimerase deficiency
Generalized GALE-D
Generalized GALE deficiency
Generalized glucocorticoid resistance syndrome
Generalized hematopoietic hypoplasia
Generalized isolated dystonia
Generalized junctional epidermolysis bullosa, non-Herlitz type
Generalized juvenile polyposis/juvenile polyposis coli
Generalized lichenoid papular eruption
Generalized lipodystrophy-progeroid features-severe intellectual disability syndrome
Generalized lymphatic anomaly
Generalized mitis RDEB
Generalized papular and sclerodermoid lichen myxedematosus
Generalized peeling skin syndrome
Generalized peeling skin syndrome type A
Generalized peeling skin syndrome type B
Generalized peeling skin syndrome type C
Generalized pseudohypoaldosteronism type 1
Generalized PSS
Generalized pustular psoriasis
Generalized resistance to thyroid hormone
Generalized UDP-galactose-4-epimerase deficiency
Generalized uridine diphosphate galactose-4-epimerase deficiency
Genetic 46,XX disorder of sex development
Genetic 46,XX DSD
Genetic 46,XY disorder of sex development
Genetic 46,XY disorder of sex development of endocrine origin
Genetic 46,XY DSD
Genetic 46,XY DSD of endocrine origin
Genetic acrokeratoderma
Genetic alopecia
Genetic anterior horn cell disease
Genetic biliary tract disease
Genetic bone tumor
Genetic brain malformation
Genetic branchial arch or oral-acral syndrome
Genetic cardiac anomaly
Genetic cardiac malformation
Genetic cardiac rhythm disease
Genetic cardiac tumor
Genetic central nervous system and retinal vascular disease
Genetic central nervous system malformation
Genetic cerebellar malformation
Genetic cerebral malformation
Genetic cerebral small vessel disease
Genetic chronic primary adrenal insufficiency
Genetic complex vascular malformation with associated anomalies
Genetic congenital limb malformation
Genetic congenital malformation of the eye with glaucoma as a major feature
Genetic corneal dystrophy
Genetic cranial malformation
Genetic craniofacial cleft
Genetic dementia
Genetic dermis disorder
Genetic dermis elastic tissue disorder
Genetic developmental defect of the eye
Genetic digestive tract malformation
Genetic digestive tract tumor
Genetic disorder of sex development
Genetic disorder of sex development of gynecological interest
Genetic DSD
Genetic DSD of gynecological interest
Genetic endocrine growth disease
Genetic epidermal appendage anomaly
Genetic epidermal disorder
Genetic epilepsy with febrile seizures-plus
Genetic erythrokeratoderma
Genetic eye tumor
Genetic facial cleft
Genetic frontotemporal degeneration with dementia
Genetic gastro-esophageal disease
Genetic glomerular disease
Genetic gynecological tumor
Genetic hair anomaly
Genetic head and neck malformation
Genetic hemoglobinopathy
Genetic hemophagocytic lymphohistiocytosis
Genetic hyperaldosteronism
Genetic hyperferritinemia without iron overload
Genetic hyperparathyroidism
Genetic hyperpigmentation of the skin
Genetic hypoparathyroidism
Genetic hypopigmentation of the skin
Genetic ichthyosis
Genetic ILD
Genetic immune deficiency with skin involvement
Genetic infertility
Genetic inflammatory or rheumatoid-like osteoarthropathy
Genetic interstitial lung disease
Genetic intestinal disease
Genetic intestinal disease due to fat malabsorption
Genetic intestinal polyposis
Genetic intractable diarrhea of infancy
Genetic larynx anomaly
Genetic lens and zonula anomaly
Genetic lethal multiple congenital anomalies/dysmorphic syndrome
Genetic lipodystrophy
Genetic malformation syndrome with odontal and/or periodontal component
Genetic malformation syndrome with short stature
Genetic MCA
Genetic MCA/variable MR
Genetic mesenchymal tumor
Genetic mixed dermis disorder
Genetic motor neuron disease
Genetic multiple congenital anomalies/dysmorphic syndrome
Genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
Genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability
Genetic multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome
Genetic multiple congenital anomalies without intellectual disability (with or without dysmorphism)
Genetic nail anomaly
Genetic neurodegenerative disease
Genetic neurodegenerative disease with dementia
Genetic neuroendocrine tumor
Genetic neurological channelopathy of the central nervous system
Genetic neurological muscular channelopathy
Genetic neuromuscular disease
Genetic neuromuscular junction disease
Genetic neuro-ophthalmological disease
Genetic neurovascular malformation
Genetic non-acquired premature ovarian failure
Genetic non-syndromic central nervous system malformation
Genetic non-syndromic obesity
Genetic non-syndromic renal or urinary tract malformation
Genetic nose and cavum anomaly
Genetic obesity
Genetic otorhinolaryngological malformation
Genetic otorhinolaryngologic disease
Genetic overgrowth/obesity syndrome
Genetic pancreatic disease
Genetic parenchymatous liver disease
Genetic periodic paralysis
Genetic peripheral neuropathy
Genetic photodermatosis
Genetic pigmentation anomaly of the skin
Genetic polycythemia
Genetic polyendocrinopathy
Genetic porokeratosis
Genetic posterior fossa malformation
Genetic precocious puberty
Genetic precocious puberty in female
Genetic primary hypomagnesemia
Genetic primary hypomagnesemia with hypocalciuria
Genetic primary hypomagnesemia with normocalciuria
Genetic primary lymphedema
Genetic primary orthostatic disorder
Genetic primary orthostatic hypotension
Genetic progeroid syndrome
Genetic recurrent myoglobinuria
Genetic renal or urinary tract malformation
Genetic renal tubular disease
Genetic renal tumor
Genetic respiratory malformation
Genetic respiratory or mediastinal malformation
Genetic sebaceous gland anomaly
Genetic skeletal muscle disease
Genetic skin photosensitivity
Genetic skin tumor
Genetic skin vascular disorder
Genetic soft tissue tumor
Genetic SRNS
Genetic steroid-resistant nephrotic syndrome
Genetic subcutaneous tissue disorder
Genetic superficial corneal dystrophy
Genetic susceptibility to infections due to particular pathogens
Genetic syndrome with a central nervous system malformation as major feature
Genetic syndrome with a cerebellar malformation as major feature
Genetic syndrome with a CNS malformation as major feature
Genetic syndrome with a Dandy-Walker malformation as major feature
Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature
Genetic syndrome with limb malformations as a major feature
Genetic syndrome with limb reduction defects
Genetic syndromic esophageal malformation
Genetic syndromic Pierre Robin syndrome
Genetic thrombotic microangiopathy
Genetic tracheal anomaly
Genetic transient congenital hypothyroidism
Genetic tumor of hematopoietic and lymphoid tissues
Genetic urogenital tract malformation
Genetic urogenital tumor
Genetic urticaria
Genetic vascular anomaly
Genetic visceral malformation of the liver, biliary tract, pancreas or spleen
Genitopalatocardiac syndrome
Genitopatellar syndrome
Genoa syndrome
Genochondromatosis type 1
Genochondromatosis type 2
Genome-wide paternal uniparental disomy mosaicism
Gentile syndrome
Genuine diffuse phlebectasia
Geographic corneal dystrophy
Geographic helicoid peripapillary choroidopathy
GEPD
GEP-NEN
Gerhardt syndrome
German syndrome
Germ cell cancer of the cervix uteri
Germ cell cancer of the corpus uteri
Germ cell tumor
Germ cell tumor of testis
Germinoma of the central nervous system
Geroderma osteodysplastica
Gershoni-Baruch-Leibo syndrome
Gershoni-Baruch syndrome
Gerstmann-Straussler-Scheinker syndrome
Gerstmann syndrome
Gestational choriocarcinoma
Gestational pemphigoid
Gestational trophoblastic disease
Gestational trophoblastic neoplasm
GET
GFM2-related combined oxidative phosphorylation defect
GFND
GH and PRL cosecreting pituitary adenoma
GHIS
Ghosal hematodiaphyseal dysplasia
Ghosal syndrome
Ghost teeth
GH receptor deficiency
Ghrelin receptor deficiency
Giant adenofibroma of the breast
Giant axonal neuropathy
Giant cell arteritis
Giant cell chondrodysplasia
Giant cell glioblastoma
Giant cell histiocytomatosis
Giant cell tumor of bone
Giant congenital melanocytic nevus
Giant hypertrophic gastritis
Giant pigmented hairy nevus
Giant platelet syndrome
Gillespie syndrome
Gingival fibromatosis-facial dysmorphism syndrome
Gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome
Gingival fibromatosis-hypertrichosis syndrome
Gingival fibromatosis-progressive deafness syndrome
Gingival hypertrophy-corneal dystrophy
GIST
GIST-paraganglioma dyad
Gitelman syndrome
Giuffré-Tsukahara syndrome
GLA
Glanzmann thrombasthenia
Glass bone disease
Glassy cell carcinoma of the cervix uteri
Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea
Glaucoma-sleep apnea syndrome
GLB1 deficiency
Glial tumor
Glial tumor of neuroepithelial tissue with unknown origin
Glioblastoma
Glioblastoma multiforme
Glioependymal/ependymal cyst
Glioma
Gliomatosis cerebri
Gliosarcoma
Global cerebellar malformation
Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome
Global developmental delay-lung cysts-overgrowth-Wilms tumor syndrome
Global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome
Global developmental delay-osteopenia-ectodermal defect syndrome
Global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome
Globodontia
Globoid cell leukodystrophy
Glomangiomatosis
Glomerular disease
Glomerulopathy with fibronectin deposits
Glomus tumor
Glomuvenous malformation
Gloomy face syndrome
Glossopalatine ankylosis
Glossopharyngeal neuralgia
GLOW syndrome
GLRX5-related sideroblastic anemia
Glucagonoma
Glucagonoma syndrome
Glucocerebrosidase deficiency
Glucocorticoid-remediable aldosteronism
Glucocorticoid-sensitive hypertension
Gluconeogenesis disorder
Glucosamine N-acetyl-6-sulfatase deficiency
Glucose-galactose malabsorption
Glucose transport disorder
Glucosidase 1 deficiency
Glucosyltransferase 1 deficiency
Glucosyltransferase 2 deficiency
Glutamate-aspartate transport defect
Glutamate-cysteine ligase deficiency
Glutamate formiminotransferase deficiency
Glutaric acidemia type 1
Glutaric acidemia type 2
Glutaric acidemia type 3
Glutaric aciduria type 1
Glutaric aciduria type 2
Glutaric aciduria type 2, mild type
Glutaric aciduria type 2, severe neonatal type
Glutaric aciduria type 3
Glutaryl-CoA dehydrogenase deficiency
Glutaryl-CoA oxidase deficiency
Glutaryl-coenzyme A dehydrogenase deficiency
Glutathione synthetase deficiency
Glutathione synthetase deficiency with 5-oxoprolinuria
Glutathione synthetase deficiency without 5-oxoprolinuria
Glutathionuria
Glycerol kinase deficiency
Glycerol kinase deficiency, adult form
Glycerol kinase deficiency-contiguous gene syndrome
Glycerol kinase deficiency, infantile form
Glycerol kinase deficiency, juvenile form
Glycine cleavage system L protein deficiency
Glycine encephalopathy
Glycine N-methyltransferase deficiency
Glycogenosis
Glycogenosis due to acid maltase deficiency
Glycogenosis due to acid maltase deficiency, infantile onset
Glycogenosis due to aldolase A deficiency
Glycogenosis due to glucose-6-phosphatase deficiency type 1a
Glycogenosis due to glucose-6-phosphatase deficiency type 1b
Glycogenosis due to glucose-6-phosphatase deficiency type Ia
Glycogenosis due to glucose-6-phosphatase transport defect type Ib
Glycogenosis due to GLUT2 deficiency
Glycogenosis due to glycogen branching enzyme deficiency
Glycogenosis due to glycogen branching enzyme deficiency, adult neuromuscular form
Glycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
Glycogenosis due to glycogen branching enzyme deficiency, childhood neuromuscular form
Glycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular form
Glycogenosis due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
Glycogenosis due to glycogen branching enzyme deficiency, non progressive hepatic form
Glycogenosis due to glycogen branching enzyme deficiency, progressive hepatic form
Glycogenosis due to glycogen debranching enzyme deficiency
Glycogenosis due to glycogen synthase deficiency
Glycogenosis due to lactate dehydrogenase deficiency
Glycogenosis due to lactate dehydrogenase H-subunit deficiency
Glycogenosis due to lactate dehydrogenase M-subunit deficiency
Glycogenosis due to LAMP-2 deficiency
Glycogenosis due to liver and muscle phosphorylase kinase deficiency
Glycogenosis due to liver glycogen phosphorylase deficiency
Glycogenosis due to liver phosphorylase kinase deficiency
Glycogenosis due to muscle and heart glycogen synthase deficiency
Glycogenosis due to muscle beta-enolase deficiency
Glycogenosis due to muscle glycogen phosphorylase deficiency
Glycogenosis due to muscle phosphofructokinase deficiency
Glycogenosis due to muscle phosphorylase kinase deficiency
Glycogenosis due to phosphoglycerate kinase 1 deficiency
Glycogenosis due to phosphoglycerate mutase deficiency
Glycogenosis due to phosphorylase kinase deficiency
Glycogenosis type 0a
Glycogenosis type 0b
Glycogenosis type 1
Glycogenosis type 11
Glycogenosis type 12
Glycogenosis type 13
Glycogenosis type 15
Glycogenosis type 1b
Glycogenosis type 2
Glycogenosis type 2, infantile onset
Glycogenosis type 2, late-onset
Glycogenosis type 3
Glycogenosis type 4
Glycogenosis type 4, adult neuromuscular form
Glycogenosis type 4, childhood combined hepatic and myopathic form
Glycogenosis type 4, childhood neuromuscular form
Glycogenosis type 4, congenital neuromuscular form
Glycogenosis type 4, fatal perinatal neuromuscular form
Glycogenosis type 4, non progressive hepatic form
Glycogenosis type 4, progressive hepatic form
Glycogenosis type 5
Glycogenosis type 6
Glycogenosis type 7
Glycogenosis type 9
Glycogenosis type 9A
Glycogenosis type 9B
Glycogenosis type 9C
Glycogenosis type 9D
Glycogenosis type 9E
Glycogenosis type I
Glycogenosis type Ia
Glycogenosis type Ib
Glycogenosis type II
Glycogenosis type III
Glycogenosis type II, infantile onset
Glycogenosis type II, late-onset
Glycogenosis type IV
Glycogenosis type IV, adult neuromuscular form
Glycogenosis type IV, childhood combined hepatic and myopathic form
Glycogenosis type IV, childhood neuromuscular form
Glycogenosis type IV, congenital neuromuscular form
Glycogenosis type IV, fatal perinatal neuromuscular form
Glycogenosis type IV, non progressive hepatic form
Glycogenosis type IV, progressive hepatic form
Glycogenosis type IX
Glycogenosis type IXa
Glycogenosis type IXb
Glycogenosis type IXc
Glycogenosis type IXd
Glycogenosis type IXe
Glycogenosis type V
Glycogenosis type VI
Glycogenosis type VII
Glycogenosis type XII
Glycogenosis type XV
Glycogenosis with hypertrophic cardiomyopathy
Glycogenosis with severe cardiomyopathy due to glycogenin deficiency
Glycogen storage disease
Glycogen storage disease due to acid maltase deficiency
Glycogen storage disease due to acid maltase deficiency, infantile onset
Glycogen storage disease due to acid maltase deficiency, late-onset
Glycogen storage disease due to aldolase A deficiency
Glycogen storage disease due to G6P deficiency
Glycogen storage disease due to G6P deficiency type Ia
Glycogen storage disease due to G6P deficiency type Ib
Glycogen storage disease due to glucose-6-phosphatase deficiency
Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia
Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib
Glycogen storage disease due to GLUT2 deficiency
Glycogen storage disease due to glycogen branching enzyme deficiency
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form
Glycogen storage disease due to glycogen debranching enzyme deficiency
Glycogen storage disease due to glycogen synthase deficiency
Glycogen storage disease due to hepatic glycogen synthase deficiency
Glycogen storage disease due to lactate dehydrogenase deficiency
Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
Glycogen storage disease due to LAMP-2 deficiency
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
Glycogen storage disease due to liver glycogen phosphorylase deficiency
Glycogen storage disease due to liver glycogen synthase deficiency
Glycogen storage disease due to liver phosphorylase kinase deficiency
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
Glycogen storage disease due to muscle beta-enolase deficiency
Glycogen storage disease due to muscle glycogen phosphorylase deficiency
Glycogen storage disease due to muscle phosphofructokinase deficiency
Glycogen storage disease due to muscle phosphorylase kinase deficiency
Glycogen storage disease due to PhK deficiency
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
Glycogen storage disease due to phosphoglycerate mutase deficiency
Glycogen storage disease due to phosphorylase kinase deficiency
Glycogen storage disease type 0a
Glycogen storage disease type 0b
Glycogen storage disease type 1
Glycogen storage disease type 11
Glycogen storage disease type 11
Glycogen storage disease type 12
Glycogen storage disease type 15
Glycogen storage disease type 1a
Glycogen storage disease type 1b
Glycogen storage disease type 2
Glycogen storage disease type 2, infantile onset
Glycogen storage disease type 2, late-onset
Glycogen storage disease type 3
Glycogen storage disease type 4
Glycogen storage disease type 4, adult neuromuscular form
Glycogen storage disease type 4, childhood combined hepatic and myopathic form
Glycogen storage disease type 4, childhood neuromuscular form
Glycogen storage disease type 4, congenital neuromuscular form
Glycogen storage disease type 4, fatal perinatal neuromuscular form
Glycogen storage disease type 4, non progressive hepatic form
Glycogen storage disease type 4, progressive hepatic form
Glycogen storage disease type 5
Glycogen storage disease type 6
Glycogen storage disease type 7
Glycogen storage disease type 9
Glycogen storage disease type 9A
Glycogen storage disease type 9B
Glycogen storage disease type 9C
Glycogen storage disease type 9D
Glycogen storage disease type 9E
Glycogen storage disease type I
Glycogen storage disease type Ib
Glycogen storage disease type II
Glycogen storage disease type III
Glycogen storage disease type II, infantile onset
Glycogen storage disease type II, late-onset
Glycogen storage disease type IV
Glycogen storage disease type IV, adult neuromuscular form
Glycogen storage disease type IV, childhood combined hepatic and myopathic form
Glycogen storage disease type IV, childhood neuromuscular form
Glycogen storage disease type IV, congenital neuromuscular form
Glycogen storage disease type IV, fatal perinatal neuromuscular form
Glycogen storage disease type IV, non progressive hepatic form
Glycogen storage disease type IV, progressive hepatic form
Glycogen storage disease type IX
Glycogen storage disease type IXa
Glycogen storage disease type IXb
Glycogen storage disease type IXc
Glycogen storage disease type IXd
Glycogen storage disease type IXe
Glycogen storage disease type V
Glycogen storage disease type VI
Glycogen storage disease type VII
Glycogen storage disease type XI
Glycogen storage disease type XII
Glycogen storage disease type XV
Glycogen storage disease with hypertrophic cardiomyopathy
Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
Glycogen storage myopathy
Glycolic aciduria
Glycoproteinosis
GM1 gangliosidosis
GM1 gangliosidosis type 1
GM1 gangliosidosis type 2
GM1 gangliosidosis type 3
GM2 gangliosidosis
GM2 gangliosidosis 0 variant
GM2 gangliosidosis, AB variant
GM2 gangliosidosis, B1 variant
GM2 gangliosidosis, B, B1 variant
GM2 gangliosidosis, B variant, adult form
GM2 gangliosidosis, B variant, infantile form
GM2 gangliosidosis, B variant, juvenile form
GM2 synthase deficiency
GM3 synthase deficiency
GMN
GMS syndrome
Gnathodiaphyseal dysplasia
GNB5-related intellectual disability-cardiac arrhythmia syndrome
GNE myopathy
GNET
GNS deficiency
Goblet cell adenocarcinoid
Goblet cell carcinoid
Goblet cell carcinoma
Goblet cell tumor
Goiter-deafness syndrome
Golabi-Rosen syndrome
Goldberg-Maxwell syndrome
Goldberg-Shprintzen megacolon syndrome
Goldberg syndrome
Goldblatt chondrodysplasia
Goldblatt syndrome
Goldblatt-Viljoen syndrome
Goldblatt-Wallis syndrome
Goldenhar syndrome
Goldmann-Favre syndrome
Goldston syndrome
Gollop syndrome
Gollop-Wolfgang complex
Goltz-Gorlin syndrome
Goltz syndrome
Gómez-López-Hernández syndrome
Gonadal dysgenesis of gynecological interest
Gonadal germ cell tumor
Gonadoblastoma
Gonadotroph adenoma
Gonadotropic deficiency
Gonadotropin-dependant precocious puberty
Gonadotropin-independent female-limited sexual precocity
Goniodysgenesis-intellectual disability-short stature syndrome
Gonococcal conjunctivitis
Gonzales-del Angel syndrome
Goodman camptodactyly
Goodman syndrome
Goodpasture syndrome
Good syndrome
Goossens-Devriendt syndrome
Gordon-Holmes syndrome
Gordon hyperkalemia-hypertension syndrome
Gordon syndrome
Gorham disease
Gorham-Stout disease
Gorham syndrome
Gorlin-Chaudhry-Moss syndrome
Gorlin-Goltz syndrome
Gorlin syndrome
GOSHS
GOSR2-related progressive myoclonus ataxia
Gottron syndrome
Gowers disease
GPA
GPAA1-related biosynthesis defect
gPAPP deficiency
GPP
GPS
GPSC
GRA
Gracile bone dysplasia
GRACILE syndrome
Graft versus host disease
Graham-Boyle-Troxell syndrome
Graham-Cox syndrome
Graham Little-Piccardi-Lassueur syndrome
Graham Little syndrome
Grange occlusive arterial syndrome
Grange syndrome
Grant syndrome
Granular corneal dystrophy type 1
Granular corneal dystrophy type 2
Granular corneal dystrophy type 3
Granular corneal dystrophy type I
Granular corneal dystrophy type II
Granular corneal dystrophy type III
Granular-lattice corneal dystrophy
Granulocytic sarcoma
Granulomatosis with polyangiitis
Granulomatous allergic angiitis
Granulomatous autoinflammatory syndrome
Granulomatous autoinflammatory syndrome of childhood
Granulomatous mastitis
Granulomatous pyoderma gangrenosum
Granulomatous slack skin
Granulosa cell cancer
Granulosa cell malignant tumor
Gravidic intrahepatic cholestasis
Gray platelet syndrome
Grayson-Wilbrandt corneal dystrophy
Greenberg dysplasia
Green jaundice
Green monkey disease
Greig cephalopolysyndactyly syndrome
Greither disease
GRFoma
GRF tumor
Grisart-Destrée syndrome
Griscelli-Pruniéras syndrome
Griscelli-Pruniéras syndrome type 1
Griscelli-Pruniéras syndrome type 2
Griscelli-Pruniéras syndrome type 3
Griscelli syndrome
Griscelli syndrome type 1
Griscelli syndrome type 2
Griscelli syndrome type 3
Groll-Hirschowitz syndrome
Gronblad-Strandberg-Touraine syndrome
Growing teratoma syndrome
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome
Growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome
Growth delay-deafness-intellectual disability syndrome
Growth delay due to insulin-like growth factor I resistance
Growth delay due to insulin-like growth factor type 1 deficiency
Growth delay-hydrocephaly-lung hypoplasia syndrome
Growth delay-intellectual disability-hepatopathy syndrome
Growth hormone and prolactin cosecreting pituitary adenoma
Growth hormone insensitivity syndrome
Growth hormone receptor deficiency
Growth hormone releasing factor tumor
Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Grubben-de Cock-Borghgraef syndrome
Grzybowski syndrome
GSD
GSD due to acid maltase deficiency
GSD due to acid maltase deficiency, infantile onset
GSD due to acid maltase deficiency, late-onset
GSD due to aldolase A deficiency
GSD due to G6P deficiency
GSD due to G6P deficiency type 1a
GSD due to G6P deficiency type 1b
GSD due to G6P deficiency type Ia
GSD due to G6P deficiency type Ib
GSD due to G6PT deficiency
GSD due to GLUT2 deficiency
GSD due to glycogen branching enzyme deficiency
GSD due to glycogen branching enzyme deficiency, adult neuromuscular form
GSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
GSD due to glycogen branching enzyme deficiency, childhood neuromuscular form
GSD due to glycogen branching enzyme deficiency, congenital neuromuscular form
GSD due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
GSD due to glycogen branching enzyme deficiency, non progressive hepatic form
GSD due to glycogen branching enzyme deficiency, progressive hepatic form
GSD due to glycogen debranching enzyme deficiency
GSD due to glycogen synthase deficiency
GSD due to hepatic glycogen synthase deficiency
GSD due to lactate dehydrogenase deficiency
GSD due to lactate dehydrogenase H-subunit deficiency
GSD due to lactate dehydrogenase M-subunit deficiency
GSD due to LAMP-2 deficiency
GSD due to liver and muscle phosphorylase kinase deficiency
GSD due to liver glycogen phosphorylase deficiency
GSD due to liver phosphorylase kinase deficiency
GSD due to muscle and heart glycogen synthase deficiency
GSD due to muscle beta-enolase deficiency
GSD due to muscle glycogen phosphorylase deficiency
GSD due to muscle phosphofructokinase deficiency
GSD due to muscle phosphorylase kinase deficiency
GSD due to phosphoglycerate kinase 1 deficiency
GSD due to phosphoglycerate mutase deficiency
GSD due to phosphorylase kinase deficiency
GSDIa
GSDIb
GSDIII
GSDIV, adult neuromuscular form
GSDIV, childhood combined hepatic and myopathic form
GSDIV, childhood neuromuscular form
GSDIV, congenital neuromuscular form
GSDIV, fatal perinatal neuromuscular form
GSDIV, non progressive hepatic form
GSDIV, progressive hepatic form
GSD type 0a
GSD type 0b
GSD type 1
GSD type 10
GSD type 11
GSD type 11
GSD type 12
GSD type 15
GSD type 1a
GSD type 1b
GSD type 1 non a
GSD type 2
GSD type 2, infantile onset
GSD type 2, late-onset
GSD type 3
GSD type 4
GSD type 4, adult neuromuscular form
GSD type 4, childhood combined hepatic and myopathic form
GSD type 4, childhood neuromuscular form
GSD type 4, congenital neuromuscular form
GSD type 4, fatal perinatal neuromuscular form
GSD type 4, non progressive hepatic form
GSD type 4, progressive hepatic form
GSD type 5
GSD type 6
GSD type 7
GSD type 9
GSD type 9A
GSD type 9B
GSD type 9C
GSD type 9D
GSD type 9E
GSD type I
GSD type Ib
GSD type II
GSD type II, infantile onset
GSD type II, late-onset
GSD type IV
GSD type IX
GSD type IXa
GSD type IXb
GSD type IXc
GSD type IXd
GSD type IXe
GSD type V
GSD type VI
GSD type VII
GSD type XI
GSD type XII
GSD type XV
GSD with hypertrophic cardiomyopathy
GSD with severe cardiomyopathy due to glycogenin deficiency
GSDXIII
GTN
GTPCH1-deficient dopa-responsive dystonia
GTPCH1-deficient DRD
GTPCH deficiency
GTP cyclohydrolase I deficiency
Guam disease
Guanarito hemorrhagic fever
Guanidinoacetate methyltransferase deficiency
Guibaud-Vainsel syndrome
Guillain-Barré-Strohl syndrome
Guillain-Barré syndrome
Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form
Guinea worm disease
Guízar Vázquez-Luengas-Muñoz syndrome
Guízar Vázquez-Sánchez-Manzano syndrome
Gunal-Seber-Basaran syndrome
Günther disease
Gurrieri-Sammito-Bellussi syndrome
Guttate hypopigmentation and punctate palmoplantar keratoderma
Guttmacher syndrome
GVH
GWCD
Gycogenosis due to PhK deficiency
Gynandroblastoma
Gyrate atrophy of choroid and retina

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