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
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Glycogen storage disease type IV, childhood neuromuscular form
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Glycogen storage disease type IV, congenital neuromuscular form
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Glycogen storage disease type IV, fatal perinatal neuromuscular form
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Glycogen storage disease type IV, non progressive hepatic form
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Glycogen storage disease type IV, progressive hepatic form
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Glycogen storage disease type IX
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Glycogen storage disease type IXa
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Glycogen storage disease type IXb
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Glycogen storage disease type IXc
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Glycogen storage disease type IXd
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Glycogen storage disease type IXe
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Glycogen storage disease type V
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Glycogen storage disease type VI
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Glycogen storage disease type VII
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Glycogen storage disease type XI
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Glycogen storage disease type XII
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Glycogen storage disease type XV
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Glycogen storage disease with hypertrophic cardiomyopathy
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Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency
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Glycogen storage myopathy
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Glycolic aciduria
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Glycoproteinosis
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GM1 gangliosidosis
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GM1 gangliosidosis type 1
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GM1 gangliosidosis type 2
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GM1 gangliosidosis type 3
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GM2 gangliosidosis
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GM2 gangliosidosis 0 variant
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GM2 gangliosidosis, AB variant
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GM2 gangliosidosis, B1 variant
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GM2 gangliosidosis, B, B1 variant
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GM2 gangliosidosis, B variant, adult form
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GM2 gangliosidosis, B variant, infantile form
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GM2 gangliosidosis, B variant, juvenile form
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GM2 synthase deficiency
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GM3 synthase deficiency
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GMN
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GMS syndrome
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Gnathodiaphyseal dysplasia
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GNB5-related intellectual disability-cardiac arrhythmia syndrome
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GNE myopathy
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GNET
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GNS deficiency
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Goblet cell adenocarcinoid
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Goblet cell carcinoid
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Goblet cell carcinoma
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Goblet cell tumor
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Goiter-deafness syndrome
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Golabi-Rosen syndrome
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Goldberg-Maxwell syndrome
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Goldberg-Shprintzen megacolon syndrome
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Goldberg syndrome
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Goldblatt chondrodysplasia
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Goldblatt syndrome
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Goldblatt-Viljoen syndrome
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Goldblatt-Wallis syndrome
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Goldenhar syndrome
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Goldmann-Favre syndrome
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Goldston syndrome
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Gollop syndrome
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Gollop-Wolfgang complex
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Goltz-Gorlin syndrome
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Goltz syndrome
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Gómez-López-Hernández syndrome
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Gonadal dysgenesis of gynecological interest
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Gonadal germ cell tumor
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Gonadoblastoma
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Gonadotroph adenoma
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Gonadotropic deficiency
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Gonadotropin-dependant precocious puberty
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Gonadotropin-independent female-limited sexual precocity
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Goniodysgenesis-intellectual disability-short stature syndrome
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Gonococcal conjunctivitis
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Gonzales-del Angel syndrome
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Goodman camptodactyly
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Goodman syndrome
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Goodpasture syndrome
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Good syndrome
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Goossens-Devriendt syndrome
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Gordon-Holmes syndrome
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Gordon hyperkalemia-hypertension syndrome
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Gordon syndrome
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Gorham disease
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Gorham-Stout disease
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Gorham syndrome
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Gorlin-Chaudhry-Moss syndrome
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Gorlin-Goltz syndrome
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Gorlin syndrome
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GOSHS
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GOSR2-related progressive myoclonus ataxia
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Gottron syndrome
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Gowers disease
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GPA
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GPAA1-related biosynthesis defect
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gPAPP deficiency
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GPP
-
GPS
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GPSC
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GRA
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Gracile bone dysplasia
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GRACILE syndrome
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Graft versus host disease
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Graham-Boyle-Troxell syndrome
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Graham-Cox syndrome
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Graham Little-Piccardi-Lassueur syndrome
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Graham Little syndrome
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Grange occlusive arterial syndrome
-
Grange syndrome
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Grant syndrome
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Granular corneal dystrophy type 1
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Granular corneal dystrophy type 2
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Granular corneal dystrophy type 3
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Granular corneal dystrophy type I
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Granular corneal dystrophy type II
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Granular corneal dystrophy type III
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Granular-lattice corneal dystrophy
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Granulocytic sarcoma
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Granulomatosis with polyangiitis
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Granulomatous allergic angiitis
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Granulomatous autoinflammatory syndrome
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Granulomatous autoinflammatory syndrome of childhood
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Granulomatous mastitis
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Granulomatous pyoderma gangrenosum
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Granulomatous slack skin
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Granulosa cell cancer
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Granulosa cell malignant tumor
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Gravidic intrahepatic cholestasis
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Gray platelet syndrome
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Grayson-Wilbrandt corneal dystrophy
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Greenberg dysplasia
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Green jaundice
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Green monkey disease
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Greig cephalopolysyndactyly syndrome
-
Greither disease
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GRFoma
-
GRF tumor
-
Grisart-Destrée syndrome
-
Griscelli-Pruniéras syndrome
-
Griscelli-Pruniéras syndrome type 1
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Griscelli-Pruniéras syndrome type 2
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Griscelli-Pruniéras syndrome type 3
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Griscelli syndrome
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Griscelli syndrome type 1
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Griscelli syndrome type 2
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Griscelli syndrome type 3
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Groll-Hirschowitz syndrome
-
Gronblad-Strandberg-Touraine syndrome
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Growing teratoma syndrome
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Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
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Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome
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Growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome
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Growth delay-deafness-intellectual disability syndrome
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Growth delay due to insulin-like growth factor I resistance
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Growth delay due to insulin-like growth factor type 1 deficiency
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Growth delay-hydrocephaly-lung hypoplasia syndrome
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Growth delay-intellectual disability-hepatopathy syndrome
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Growth hormone and prolactin cosecreting pituitary adenoma
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Growth hormone insensitivity syndrome
-
Growth hormone receptor deficiency
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Growth hormone releasing factor tumor
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Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome
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Growth retardation-mild developmental delay-chronic hepatitis syndrome
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Grubben-de Cock-Borghgraef syndrome
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Grzybowski syndrome
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GSD
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GSD due to acid maltase deficiency
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GSD due to acid maltase deficiency, infantile onset
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GSD due to acid maltase deficiency, late-onset
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GSD due to aldolase A deficiency
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GSD due to G6P deficiency
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GSD due to G6P deficiency type 1a
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GSD due to G6P deficiency type 1b
-
GSD due to G6P deficiency type Ia
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GSD due to G6P deficiency type Ib
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GSD due to G6PT deficiency
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GSD due to GLUT2 deficiency
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GSD due to glycogen branching enzyme deficiency
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GSD due to glycogen branching enzyme deficiency, adult neuromuscular form
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GSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
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GSD due to glycogen branching enzyme deficiency, childhood neuromuscular form
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GSD due to glycogen branching enzyme deficiency, congenital neuromuscular form
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GSD due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form
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GSD due to glycogen branching enzyme deficiency, non progressive hepatic form
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GSD due to glycogen branching enzyme deficiency, progressive hepatic form
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GSD due to glycogen debranching enzyme deficiency
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GSD due to glycogen synthase deficiency
-
GSD due to hepatic glycogen synthase deficiency
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GSD due to lactate dehydrogenase deficiency
-
GSD due to lactate dehydrogenase H-subunit deficiency
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GSD due to lactate dehydrogenase M-subunit deficiency
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GSD due to LAMP-2 deficiency
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GSD due to liver and muscle phosphorylase kinase deficiency
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GSD due to liver glycogen phosphorylase deficiency
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GSD due to liver phosphorylase kinase deficiency
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GSD due to muscle and heart glycogen synthase deficiency
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GSD due to muscle beta-enolase deficiency
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GSD due to muscle glycogen phosphorylase deficiency
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GSD due to muscle phosphofructokinase deficiency
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GSD due to muscle phosphorylase kinase deficiency
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GSD due to phosphoglycerate kinase 1 deficiency
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GSD due to phosphoglycerate mutase deficiency
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GSD due to phosphorylase kinase deficiency
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GSDIa
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GSDIb
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GSDIII
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GSDIV, adult neuromuscular form
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GSDIV, childhood combined hepatic and myopathic form
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GSDIV, childhood neuromuscular form
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GSDIV, congenital neuromuscular form
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GSDIV, fatal perinatal neuromuscular form
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GSDIV, non progressive hepatic form
-
GSDIV, progressive hepatic form
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GSD type 0a
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GSD type 0b
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GSD type 1
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GSD type 10
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GSD type 11
-
GSD type 11
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GSD type 12
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GSD type 15
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GSD type 1a
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GSD type 1b
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GSD type 1 non a
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GSD type 2
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GSD type 2, infantile onset
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GSD type 2, late-onset
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GSD type 3
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GSD type 4
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GSD type 4, adult neuromuscular form
-
GSD type 4, childhood combined hepatic and myopathic form
-
GSD type 4, childhood neuromuscular form
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GSD type 4, congenital neuromuscular form
-
GSD type 4, fatal perinatal neuromuscular form
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GSD type 4, non progressive hepatic form
-
GSD type 4, progressive hepatic form
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GSD type 5
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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
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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
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GSD with hypertrophic cardiomyopathy
-
GSD with severe cardiomyopathy due to glycogenin deficiency
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GSDXIII
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GTN
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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