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G6PD ( Glucose-6-phosphate-dehydrogenase deficiency [3] )
GA I ( Glutaric acidemia I [25] )
GABEB ( Epidermolysis bullosa, junctional, non-Herlitz type [5] )
GACI ( Arterial calcification, generalized, of infancy [9] )
GALK deficiency ( Galactokinase deficiency [1] )
GALNS deficiency ( Mucopolysaccharidosis, type IVA [1] )
GALT deficiency ( Galactosemia [4] )
GAN ( Giant axonal neuropathy 1 [13] )
GAN1 ( Giant axonal neuropathy 1 [13] )
GAPO syndrome [6]
GBE1 deficiency ( Glycogen storage disease IV [1] )
GCCD2 ( Glucocorticoid deficiency 2 [4] )
GCD1 ( Groenouw type I corneal dystrophy [5] )
GCE ( Glycine encephalopathy [8] )
GCL ( Krabbe disease [47] )
GCPS ( Greig cephalopolysyndactyly syndrome [2] )
GD I ( Gaucher disease, type I [21] )
GD II ( Gaucher disease, type II [1] )
GD III ( Gaucher disease, type III [3] )
GDD ( Gnathodiaphyseal dysplasia [1] )
GDLD ( Corneal dystrophy, gelatinous drop-like [31] )
GDXY ( Swyer syndrome [6] )
GGF1 ( Fibromatosis, gingival, 1 [1] )
GINGF ( Fibromatosis, gingival, 1 [1] )
GINGF1 ( Fibromatosis, gingival, 1 [1] )
GIST ( Carney-Stratakis syndrome [2] )
GLB1 deficiency ( Gangliosidosis, generalized GM1, type I [1] )
GLC1A ( Glaucoma, primary open angle, juvenile-onset, 1 [5] )
GLC1H ( Glaucoma 1, open angle, H [1] )
GLC3 ( Glaucoma 3, primary congenital, A [9] )
GLC3A ( Glaucoma 3, primary congenital, A [9] )
GLUT1 deficiency syndrome [2]
GM1-gangliosidosis, type I ( Gangliosidosis, generalized GM1, type I [1] )
GM2 gangliosidosis, type I ( Tay-Sachs disease [6] )
GM2 gangliosidosis, type II ( Sandhoff disease [2] )
GOSHS ( Goldberg-Shprintzen megacolon syndrome [2] )
GP IIb-IIIa complex, deficiency of ( Glanzmann thrombasthenia [9] )
GRD ( Graves disease [18] )
GSD ( Gerstmann-Sträussler disease [7] )
GSD IIb ( Danon disease [18] )
GSD IV ( Glycogen storage disease IV [1] )
GSD1B ( Glycogen storage disease Ib [9] )
GSD2B ( Danon disease [18] )
GSH ( Glucocorticoid-remediable aldosteronism [1] )
GSSD ( Gerstmann-Sträussler disease [7] )
GT ( Glanzmann thrombasthenia [9] )
GTS ( Gilles de la Tourette syndrome [29] )
GUSB deficiency ( Mucopolysaccharidosis, type VII [3] )
GVM ( Glomuvenous malformations [13] )
Galactocerebrosidase deficiency ( Krabbe disease [47] )
Galactokinase deficiency [1]
Galactosamine-6-sulfatase deficiency ( Mucopolysaccharidosis, type IVA [1] )
Galactose-1-phosphate uridyl-transferase deficiency ( Galactosemia [4] )
Galactosemia [4]
Galactosemia II ( Galactokinase deficiency [1] )
Galactosemia, classic ( Galactosemia [4] )
Galactosylceramide beta-galactosidase deficiency ( Krabbe disease [47] )
Gallbladder agenesis [7]
Gallbladder duplication [2]
Ganglioneuromatosis of the alimentary tract ( Multiple endocrine neoplasia, type IIB [5] )
Gangliosidosis, generalized GM1, infantile form ( Gangliosidosis, generalized GM1, type I [1] )
Gangliosidosis, generalized GM1, type I [1]
Gardner syndrome ( Adenomatous polyposis of the colon [20] )
Gartner duct cyst [14]
Gastric duplication [16]
Gastric teratoma [9]
Gastroenteric duplication cyst [2]
Gastroschisis [4]
Gastroschisis - Prenatal diagnosis [20]
Gastroschisis repair [11]
Gaucher disease [19]
Gaucher disease, acute neuronopathic type ( Gaucher disease, type II [1] )
Gaucher disease, chronic neuronopathic type ( Gaucher disease, type III [3] )
Gaucher disease, infantile cerebral ( Gaucher disease, type II [1] )
Gaucher disease, juvenile and adult, cerebral ( Gaucher disease, type III [3] )
Gaucher disease, noncerebral juvenile ( Gaucher disease, type I [21] )
Gaucher disease, subacute neuronopathic type ( Gaucher disease, type III [3] )
Gaucher disease, type I [21]
Gaucher disease, type II [1]
Gaucher disease, type III [3]
Gaze palsy, familial horizontal, with progressive scoliosis [8]
Geleophysic dwarfism ( Geleophysic dysplasia [5] )
Geleophysic dysplasia [5]
Gene map locus 12q13 ( Epidermolysis bullosa simplex with migratory circinate erythema [2] )
Gene map locus 13pter-q12.13 ( Corneal dystrophy, Fuchs endothelial, 2 [3] )
Gene map locus 13q12.11 ( Fibrosis of extraocular muscles, congenital, 3C [1] )
Gene map locus 16q11.1-q22 ( Dupuytren contracture [3] )
Gene map locus 16q22.1 ( EEM syndrome [1] )
Gene map locus 17q21 ( Neutropenia, severe congenital, autosomal recessive 4 [1] )
Gene map locus 1p32 ( Ceroid lipofuscinosis, neuronal, 1 [5] )
Gene map locus 1q21.1 ( Cataract-microcornea syndrome [2] )
Gene map locus 7q22.1 ( Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form [2] )
Generalized arterial calcification of infancy ( Arterial calcification, generalized, of infancy [9] )
Generalized resistance to 1,25-dihydroxyvitamin D ( Vitamin D-dependent rickets, type 2A [2] )
Genitopatellar syndrome [5]
Geographic tongue [8]
Geographic tongue and fissured tongue ( Geographic tongue [8] )
German type amyloidosis ( Amyloidosis, familial visceral [3] )
Germinal cell aplasia ( Sertoli cell-only syndrome [18] )
Gerstmann-Straussler-Scheinker disease ( Gerstmann-Sträussler disease [7] )
Gerstmann-Sträussler disease [7]
Giant axonal neuropathy 1 [13]
Giant platelet syndrome ( Bernard-Soulier syndrome [3] )
Gigantism, partial, of hands and feet, nevi, hemihypertrophy, and macrocephaly ( Proteus syndrome [24] )
Gilles de la Tourette syndrome [29]
Gingival neoplasm ( Epulis, congenital [15] )
Gitelman syndrome [4]
Glanzmann thrombasthenia [9]
Glanzmann thrombasthenia - Dental anomalies [5]
Glaucoma 1, open angle, A ( Glaucoma, primary open angle, juvenile-onset, 1 [5] )
Glaucoma 1, open angle, H [1]
Glaucoma 3, primary congenital, A [9]
Glaucoma, congenital ( Glaucoma 3, primary congenital, A [9] )
Glaucoma, primary open angle, juvenile-onset, 1 [5]
Globoid cell leukodystrophy ( Krabbe disease [47] )
Globoid cell leukoencephalopathy ( Krabbe disease [47] )
Glomangiomas, multiple ( Glomuvenous malformations [13] )
Glomerulocystic kidney disease [8]
Glomerulonephritis with isolated C3 deposits and factor H deficiency ( Complement factor H deficiency [7] )
Glomerulosclerosis, focal segmental ( Focal segmental glomerulosclerosis 1 [1] )
Glomerulosclerosis, focal segmental, 1 ( Focal segmental glomerulosclerosis 1 [1] )
Glomus tumors, multiple ( Glomuvenous malformations [13] )
Glomuvenous malformations [13]
Gloomy face syndrome ( Three M syndrome 1 [3] )
Glossitis areata exfoliativa ( Geographic tongue [8] )
Glossitis, benign migratory ( Geographic tongue [8] )
Glossoptosis, micrognathia, and cleft palate ( Pierre Robin syndrome [18] )
Glucocerebrosidase deficiency ( Gaucher disease [19] )
Glucocerebrosidase deficiency ( Gaucher disease, type I [21] )
Glucocorticoid deficiency 2 [4]
Glucocorticoid deficiency and achalasia ( Triple-A syndrome [10] )
Glucocorticoid-remediable aldosteronism [1]
Glucocorticoid-suppressible hyperaldosteronism ( Glucocorticoid-remediable aldosteronism [1] )
Glucose transport defect, blood-brain barrier ( GLUT1 deficiency syndrome [2] )
Glucose-6-phosphatase deficiency ( Glycogen storage disease I [3] )
Glucose-6-phosphate transport defect ( Glycogen storage disease Ib [9] )
Glucose-6-phosphate-dehydrogenase deficiency [3]
Glucosidase, acid, alpha deficiency ( Glycogen storage disease II [12] )
Glutaric acidemia I [25]
Glutaric aciduria I ( Glutaric acidemia I [25] )
Glutaryl-CoA dehydrogenase deficiency ( Glutaric acidemia I [25] )
Glutathione synthetase deficiency [1]
Gluten enteropathy ( Celiac disease [18] )
Gluten-induced enteropathy ( Celiac disease [18] )
Gluten-sensitive enteropathy ( Celiac disease [18] )
Glyceric aciduria ( Hyperoxaluria, primary, type II [2] )
Glycine encephalopathy [8]
Glycogen branching enzyme deficiency ( Glycogen storage disease IV [1] )
Glycogen storage cardiomyopathy ( Danon disease [18] )
Glycogen storage disease I [3]
Glycogen storage disease II [12]
Glycogen storage disease IIb ( Danon disease [18] )
Glycogen storage disease IV [1]
Glycogen storage disease Ia ( Glycogen storage disease I [3] )
Glycogen storage disease Ib [9]
Glycogen storage disease V [13]
Glycogen storage disease XI ( Fanconi-Bickel syndrome [3] )
Glycogen storage disease limited to the heart ( Danon disease [18] )
Glycogen storage disease of heart ( Glycogen storage disease of heart, lethal congenital [1] )
Glycogen storage disease of heart, lethal congenital [1]
Glycogenosis IV ( Glycogen storage disease IV [1] )
Glycogenosis, Fanconi type ( Fanconi-Bickel syndrome [3] )
Glycolic aciduria ( Hyperoxaluria, primary, type I [30] )
Glycoprotein complex IIb-IIIa, deficiency of ( Glanzmann thrombasthenia [9] )
Glycoprotein neuraminidase deficiency ( Neuraminidase deficiency [4] )
Glycosylasparaginase deficiency ( Aspartylglucosaminuria [8] )
Glyoxylate reductase/hydroxypyruvate reductase deficiency ( Hyperoxaluria, primary, type II [2] )
Gnathodiaphyseal dysplasia [1]
Gnathodiaphyseal sclerosis ( Gnathodiaphyseal dysplasia [1] )
Goiter, dyshormonogenetic [10]
Goiter-deafness syndrome ( Pendred syndrome [8] )
Golabi-Ito-Hall syndrome [1]
Golabi-Rosen syndrome ( Simpson-Golabi-Behmel syndrome [2] )
Goldberg-Shprintzen megacolon syndrome [2]
Goldenhar syndrome [37]
Goldenhar syndrome - Dental anomalies [14]
Goldenhar syndrome - Eyes [7]
Goldenhar syndrome - Imaging [25]
Goldenhar syndrome with ipsilateral radial defect ( Hemifacial microsomia with radial defects [14] )
Goldmann-Favre syndrome [1]
Goldston syndrome ( Renal-hepatic-pancreatic dysplasia [5] )
Goltz syndrome ( Focal dermal hypoplasia [25] )
Goltz-Gorlin syndrome ( Focal dermal hypoplasia [25] )
Gonadal dysgenesis, 45,X ( Turner syndrome [31] )
Gonadal dysgenesis, XY female type ( Swyer syndrome [6] )
Gordon Holmes syndrome ( Cerebellar ataxia and hypogonadotropic hypogonadism [4] )
Gorlin syndrome [14]
Gorlin syndrome - Dental anomalies [8]
Gorlin syndrome - Histology [5]
Gorlin syndrome - Imaging [17]
Gorlin-Goltz syndrome ( Gorlin syndrome [14] )
Granular cell tumor of the newborn ( Epulis, congenital [15] )
Granular corneal dystrophy, type I ( Groenouw type I corneal dystrophy [5] )
Granular corneal dystrophy, type II ( Corneal dystrophy, Avellino type [10] )
Granulomatosis, familial juvenile systemic ( Blau syndrome [9] )
Granulomatosis, familial, Blau type ( Blau syndrome [9] )
Granulomatous inflammatory arthritis, dermatitis, and uveitis, familial ( Blau syndrome [9] )
Graves disease [18]
Graves disease - Pretibial myxedema [8]
Graves ophthalmopathy [23]
Graves ophthalmopathy - Histology [1]
Graves ophthalmopathy - Imaging [17]
Grebe chondrodysplasia ( Chondrodysplasia, Grebe type [3] )
Grebe dysplasia ( Chondrodysplasia, Grebe type [3] )
Greenberg dysplasia ( Hydrops-ectopic calcification-moth-eaten skeletal dysplasia [2] )
Greenfield disease ( Metachromatic leukodystrophy [22] )
Greig cephalopolysyndactyly syndrome [2]
Greig syndrome ( Greig cephalopolysyndactyly syndrome [2] )
Greither disease ( Erythrokeratodermia variabilis [45] )
Griscelli syndrome [11]
Griscelli syndrome - Dental anomalies [5]
Groenouw type I corneal dystrophy [5]
Groenouw type II corneal dystrophy ( Macular corneal dystrophy [20] )
Gronblad-Strandberg syndrome ( Pseudoxanthoma elasticum [29] )
Growth hormone insensitivity syndrome ( Laron syndrome [17] )
Growth hormone receptor deficiency ( Laron syndrome [17] )
Growth retardation with sensorineural deafness and mental retardation ( Insulin-like growth factor I deficiency [1] )
Growth retardation, alopecia, pseudoanodontia, and optic atrophy ( GAPO syndrome [6] )
Growth-mental deficiency syndrome of Myhre ( Myhre syndrome [4] )
Gruber syndrome ( Meckel syndrome [1] )
Guibaud-Vainsel syndrome ( Osteopetrosis, autosomal recessive 3 [11] )
Gunther disease ( Porphyria, congenital erythropoietic [24] )
Gyrate atrophy [4]
Gyrate atrophy of the choroid and retina ( Gyrate atrophy [4] )
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Edited by Aldo Campana, August 21, 2012
