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973 Result(s)
- G-PDC
- G6P deficiency
- G6P deficiency type 1a
- G6P deficiency type Ib
- G6P translocase deficiency
- G6PT deficiency
- GA1
- GABA transaminase deficiency
- Gabriele-de Vries syndrome
- Gaisböck syndrome
- Galactocerebrosidase deficiency
- Galactokinase deficiency
- Galactokinase deficiency galactosemia
- Galactosamine-6-sulfatase deficiency
- Galactose epimerase deficiency
- Galactose mutarotase deficiency
- Galactose-1-phosphate uridyltransferase deficiency
- Galactosemia
- Galactosemia type 1
- Galactosemia type 2
- Galactosemia type 3
- Galactosemia type 4
- Galactosialidosis
- Galactosylceramidase deficiency
- GALC deficiency
- GALE deficiency
- GALE-D
- GALK deficiency
- GALK-D
- Gallbladder neuroendocrine tumor
- Gallblader arteriovenous malformation
- Galloway syndrome
- Galloway-Mowat syndrome
- GALM deficiency
- GALNS deficiency
- GALT deficiency
- Game-Friedman-Paradice syndrome
- Gamma-aminobutyric acid transaminase deficiency
- Gamma-cystathionase deficiency
- Gamma-glutamyl transferase deficiency
- Gamma-glutamyl transpeptidase deficiency
- Gamma-glutamylcysteine synthetase deficiency
- Gamma-HCD
- Gamma-heavy chain disease
- Gamma-hydroxybutyric aciduria
- Gamma-sarcoglycan-related LGMD R5
- Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5
- Gamma-sarcoglycanopathy
- Gamstorp disease
- Gamstorp episodic adynamy
- GAMT deficiency
- GAN
- Gangliocytoma
- Ganglioglioma
- Ganglioneuroblastoma
- Ganglioneuroma
- Gangliosidosis
- GAPO syndrome
- GAPPS
- Garcia-Lurie syndrome
- Gardner syndrome
- Gardner-Diamond syndrome
- Gardner-Silengo-Wachtel 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
- Gastrointestinal tract arteriovenous malformation
- Gastroschisis
- GATA binding protein 2 deficiency spectrum
- GATA2 deficiency spectrum
- Gaucher disease
- Gaucher disease type 1
- Gaucher disease type 2
- Gaucher disease type 3
- Gaucher disease type 3C
- Gaucher disease, subacute neuronopathic type
- Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome
- 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
- GCL4
- GCM syndrome
- GCP-CGS
- GCPS
- GCT of bone
- GDCD
- GDD
- GDE deficiency
- GDS
- GEFS+
- GEKA
- Gelastic seizures with hypothalamic hamartoma
- Gelatinous ascites
- Gelatinous drop-like corneal dystrophy
- Geleophysic dwarfism
- Geleophysic dysplasia
- Gelsolin amyloidosis
- Gemignani syndrome
- Gemistocytic astrocytoma
- GEMSS syndrome
- Generalized arterial calcification of infancy
- Generalized atrophic benign epidermolysis bullosa
- Generalized basaloid follicular hamartoma syndrome
- Generalized bulbospinal muscular atrophy
- Generalized cervical and upper-limb-onset dystonia
- Generalized DDEB
- Generalized deciduous skin
- Generalized epilepsy with febrile seizures plus
- Generalized epilepsy-paroxysmal dyskinesia syndrome
- 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 deficiency
- Generalized GALE-D
- Generalized glucocorticoid resistance syndrome
- 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 lymphatic dysplasia of Fotiou
- Generalized papular and sclerodermoid lichen myxedematosus
- Generalized peeling skin disease type B
- Generalized peeling skin syndrome
- Generalized peeling skin syndrome type A
- Generalized peeling skin syndrome type B
- Generalized PHA1
- Generalized pseudohypoaldosteronism type 1
- Generalized PSS
- Generalized pustular psoriasis
- Generalized RDEB, intermediate form
- Generalized RDEB, severe form
- Generalized UDP-galactose-4-epimerase deficiency
- Generalized uridine diphosphate galactose-4-epimerase deficiency
- Genetic 46,XX difference of sex development
- Genetic 46,XX disorder of sex development
- Genetic 46,XX DSD
- Genetic 46,XY difference of sex development
- Genetic 46,XY difference of sex development of endocrine origin
- 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 autoinflammatory syndrome with acne and/or hidradenitis suppurativa
- Genetic autoinflammatory syndrome with skin involvement
- 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 central precocious puberty
- Genetic central precocious puberty in boy
- Genetic central precocious puberty in female
- Genetic central precocious puberty in girl
- Genetic central precocious puberty in male
- 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 CPP
- Genetic CPP in boy
- Genetic CPP in female
- Genetic CPP in girl
- Genetic CPP in male
- Genetic cranial malformation
- Genetic craniofacial cleft
- Genetic cystic renal disease
- Genetic dementia
- Genetic dermis disorder
- Genetic dermis elastic tissue disorder
- Genetic developmental defect of the eye
- Genetic difference of sex development
- Genetic difference of sex development of gynecological interest
- 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 seizure plus
- Genetic erythrokeratoderma
- Genetic eye tumor
- Genetic facial cleft
- Genetic frontotemporal degeneration with dementia
- Genetic FSGS
- Genetic gastro-esophageal disease
- Genetic glomerular disease
- Genetic gynecological tumor
- Genetic hair anomaly
- Genetic head and neck malformation
- Genetic hemangiolymphangioma
- Genetic hemoglobinopathy
- Genetic hemolytic uremic syndrome
- Genetic hemophagocytic lymphohistiocytosis
- Genetic hemophagocytic lymphohistiocytosis with hypopigmentation
- Genetic hemophagocytic lymphohistiocytosis without hypopigmentation
- Genetic HLH
- Genetic HLH with hypopigmentation
- Genetic HLH without hypopigmentation
- Genetic human prion disease
- Genetic HUS
- 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 mesenchymal tumor
- Genetic mixed dermis disorder
- Genetic motor neuron disease
- Genetic multiple congenital anomalies without intellectual disability (with or without dysmorphism)
- Genetic multiple congenital anomalies-intellectual disability with or without dysmorphism
- Genetic multiple congenital anomalies/dysmorphic syndrome
- Genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Genetic multiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Genetic nail anomaly
- Genetic nephrotic syndrome
- Genetic neuro-ophthalmological disease
- 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 neurovascular malformation
- 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 otorhinolaryngologic disease
- Genetic otorhinolaryngological malformation
- Genetic overgrowth/obesity syndrome
- Genetic pancreatic disease
- Genetic panhypopituitarism
- 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 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 or hamartoma
- Genetic skin vascular disorder
- Genetic soft tissue tumor
- Genetic SRNS
- 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 a major feature
- Genetic syndrome with a cerebellar malformation as a major feature
- Genetic syndrome with a CNS malformation as major feature
- Genetic syndrome with a Dandy-Walker malformation as a 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 systemic disease with glomerulopathy as a major feature
- 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
- GEP-NEN
- GEPD
- Gerhardt syndrome
- Germ cell cancer of the cervix uteri
- Germ cell cancer of the corpus uteri
- Germ cell tumor
- Germ cell tumor of testis
- German syndrome
- Germinoma of the central nervous system
- Geroderma osteodysplastica
- Gershoni-Baruch syndrome
- Gershoni-Baruch-Leibo syndrome
- Gerstmann syndrome
- Gerstmann-Straussler-Scheinker syndrome
- Gestational choriocarcinoma
- Gestational pemphigoid
- Gestational trophoblastic disease
- Gestational trophoblastic neoplasm
- GET
- GFM2-related combined oxidative phosphorylation defect
- GFND
- GGM
- GH and PRL cosecreting pituitary adenoma
- GH receptor deficiency
- GHIS
- Ghosal hematodiaphyseal dysplasia
- Ghosal syndrome
- Ghost teeth
- Ghrelin receptor deficiency
- GI arteriovenous malformation
- 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 hypertrophic gastritis
- Giant omphalocele
- Giant platelet syndrome
- Gillespie syndrome
- Gingival fibromatosis-aortic root dilatation-facial dysmorphism-intellectual disability syndrome
- Gingival fibromatosis-facial dysmorphism syndrome
- Gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome
- Gingival fibromatosis-hypertrichosis syndrome
- Gingival fibromatosis-progressive deafness syndrome
- Gingival fibromatosis-progressive hearing loss syndrome
- Gingival hypertrophy-corneal dystrophy
- GIST
- GIST-paraganglioma dyad
- Gitelman syndrome
- Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation
- Gitelman-like kidney tubulopathy due to mtDNA mutation
- Giuffré-Tsukahara syndrome
- GJC2-related late-onset primary lymphedema
- GLA
- Glanders
- Glanzmann thrombasthenia
- Glass bone disease
- Glassy cell carcinoma of the cervix uteri
- Glaucoma secondary to spherophakia/ectopia lentis and megalocornea
- Glaucoma-ectopia lentis-microspherophakia-stiff joints-short stature syndrome
- Glaucoma-sleep apnea syndrome
- Glaucomatocyclitic crisis disease
- 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-hypotonia-high pain tolerance syndrome
- Global developmental delay-intellectual disability-facial dysmorphism-pseudo-Pelger-Huët anomaly 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
- Glossopalatine ankylosis
- Glossopharyngeal neuralgia
- GLOW syndrome
- GLRX5-related sideroblastic anemia
- Glucagonoma
- Glucagonoma syndrome
- Glucocerebrosidase deficiency
- Glucocorticoid-remediable aldosteronism
- Glucocorticoid-sensitive hypertension
- Glucokinase-related hyperinsulinemic hypoglycemia
- Gluconeogenesis disorder
- Glucosamine N-acetyl-6-sulfatase deficiency
- Glucose transport disorder
- Glucose-6-phosphate isomerase deficiency
- Glucose-galactose malabsorption
- Glucosidase 1 deficiency
- Glucosyltransferase 1 deficiency
- Glucosyltransferase 2 deficiency
- Glutamate formiminotransferase deficiency
- Glutamate-aspartate transport defect
- Glutamate-cysteine ligase 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, juvenile form
- Glycine cleavage system L protein deficiency
- Glycine encephalopathy
- Glycine N-methyltransferase 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 PGAM2 deficiency
- Glycogen storage disease due to PhK deficiency
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- Glycogen storage disease due to phosphoglycerate mutase 2 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 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 II, infantile onset
- Glycogen storage disease type II, late-onset
- Glycogen storage disease type III
- 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 XII
- Glycogen storage disease type XV
- Glycogen storage disease with hypertrophic cardiomyopathy
- Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
- Glycogen storage disease, type 10
- Glycogen storage disease, type 2B
- Glycogen storage disease, type IIb
- Glycogen storage disease, type X
- Glycogen storage myopathy
- 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 2 deficiency
- Glycogenosis due to phosphorylase kinase deficiency
- Glycogenosis type 0a
- Glycogenosis type 0b
- Glycogenosis type 1
- 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 II, infantile onset
- Glycogenosis type II, late-onset
- Glycogenosis type III
- 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
- Glycolic aciduria
- Glycoproteinosis
- GM1 gangliosidosis
- GM1 gangliosidosis type 1
- GM1 gangliosidosis type 2
- GM1 gangliosidosis type 3
- GM2 gangliosidosis
- GM2 gangliosidosis, AB variant
- GM2 gangliosidosis, hexosaminidase A and B deficiency variant, adult form
- GM2 gangliosidosis, hexosaminidase A and B deficiency variant, infantile form
- GM2 gangliosidosis, hexosaminidase A and B deficiency variant, juvenile form
- GM2 gangliosidosis, hexosaminidase A deficiency variant
- GM2 gangliosidosis, hexosaminidase A deficiency variant, adult form
- GM2 gangliosidosis, hexosaminidase A deficiency variant, infantile form
- GM2 gangliosidosis, Hexosaminidase A deficiency variant, juvenile form
- GM2 gangliosidosis, Sandhoff variant, adult form
- GM2 gangliosidosis, Sandhoff variant, infantile form
- GM2 gangliosidosis, Sandhoff variant, juvenile form
- GM2 gangliosidosis, Tay-Sachs variant
- GM2 gangliosidosis, Tay-Sachs variant, adult form
- GM2 gangliosidosis, Tay-Sachs variant, infantile form
- GM2 gangliosidosis, Tay-Sachs variant, juvenile form
- GM2 synthase deficiency
- GM3 synthase deficiency
- GMPPB-related LGMD R19
- GMPPB-related limb-girdle muscular dystrophy R19
- GMS syndrome
- GNAO1-related developmental delay-seizures-movement disorder spectrum
- GNAO1-related neurodevelopmental disorder
- GNAO1-related spectrum
- 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
- Goiter-hearing loss syndrome
- Golabi-Rosen syndrome
- Goldberg syndrome
- Goldberg-Maxwell syndrome
- Goldberg-Shprintzen megacolon syndrome
- Goldblatt chondrodysplasia
- Goldblatt syndrome
- Goldblatt-Viljoen syndrome
- Goldblatt-Wallis syndrome
- Goldmann-Favre syndrome
- Goldston syndrome
- Gollop syndrome
- Gollop-Wolfgang complex
- Goltz syndrome
- Goltz-Gorlin syndrome
- Gonadal dysgenesis of gynecological interest
- Gonadal germ cell tumor
- Gonadoblastoma
- Gonadotroph adenoma
- Gonadotropic deficiency
- Gonadotropin-dependant precocious puberty
- Goniodysgenesis-intellectual disability-short stature syndrome
- Gonococcal conjunctivitis
- Gonzales-del Angel syndrome
- Good syndrome
- Goodman camptodactyly
- Goossens-Devriendt syndrome
- Gordon hyperkalemia-hypertension syndrome
- Gordon syndrome
- Gordon-Holmes syndrome
- Gorham disease
- Gorham syndrome
- Gorham-Stout disease
- Gorlin syndrome
- Gorlin-Chaudhry-Moss syndrome
- Gorlin-Goltz syndrome
- GOSHS
- GOSR2-related progressive myoclonus ataxia
- Gottron syndrome
- GPA
- GPAA1-related biosynthesis defect
- gPAPP deficiency
- GPI deficiency
- GPP
- GPS
- GPSC
- GRA
- Gracile bone dysplasia
- GRACILE syndrome
- Graft versus host disease
- Graham Little syndrome
- Graham Little-Piccardi-Lassueur syndrome
- Graham-Boyle-Troxell syndrome
- Graham-Cox 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
- Granuloma faciale
- Granuloma of Lever
- 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
- Green jaundice
- Green monkey disease
- Greenberg dysplasia
- Greig cephalopolysyndactyly syndrome
- Greig cephalopolysyndactyly-contiguous gene syndrome
- Greither disease
- GRF tumor
- GRFoma
- GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
- GRIN2B-Related Neurodevelopmental Disorder
- Grisart-Destrée syndrome
- Griscelli syndrome
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Griscelli-Pruniéras syndrome
- Griscelli-Pruniéras syndrome type 1
- Griscelli-Pruniéras syndrome type 2
- Griscelli-Pruniéras syndrome type 3
- Grisel syndrome
- Groll-Hirschowitz syndrome
- Gronblad-Strandberg-Touraine syndrome
- Growing teratoma syndrome
- Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
- Growth delay due to insulin-like growth factor I resistance
- Growth delay due to insulin-like growth factor type 1 deficiency
- Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome
- Growth delay-deafness-intellectual disability syndrome
- Growth delay-hearing loss-intellectual disability syndrome
- 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
- GS-HH
- 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 2 deficiency
- GSD due to phosphorylase kinase deficiency
- GSD type 0a
- GSD type 0b
- GSD type 1
- GSD type 1 non a
- GSD type 10
- GSD type 12
- GSD type 15
- GSD type 1a
- GSD type 1b
- 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 XII
- GSD type XV
- GSD with hypertrophic cardiomyopathy
- GSD with severe cardiomyopathy due to glycogenin deficiency
- GSD, type 2B
- GSD, type IIb
- 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
- GSDXIII
- GTCA
- GTN
- GTP cyclohydrolase I deficiency
- GTPCH deficiency
- GTPCH1-deficient dopa-responsive dystonia
- GTPCH1-deficient DRD
- Guam disease
- Guam parkinsonism-dementia complex
- Guanarito hemorrhagic fever
- Guanidinoacetate methyltransferase deficiency
- Guibaud-Vainsel syndrome
- Guillain-Barré syndrome
- Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form
- Guillain-Barré-Strohl syndrome
- Guinea worm disease
- Gurrieri-Sammito-Bellussi syndrome
- Gustatory hyperhidrosis
- Guttate hypopigmentation and punctate palmoplantar keratoderma
- Guttmacher syndrome
- Guízar Vázquez-Luengas-Muñoz syndrome
- Guízar Vázquez-Sánchez-Manzano syndrome
- GvHD
- GWCD
- Gycogenosis due to PhK deficiency
- Gynandroblastoma
- Gyrate atrophy of choroid and retina
- Gélineau disease
- Gómez-López-Hernández syndrome
- Günther disease