About
Site Map
Contact Us
A service of the
U.S. National Library of Medicine®
Home
Conditions
Genes
Chromosomes
Handbook
Glossary
Resources
Genetic Conditions
>
Browse Conditions
A
|
B
|
C
|
D
|
E
|
F
|
G
|
H
|
I
|
J
|
K
|
L
|
M
|
N
|
O
|
P
|
Q-R
|
S
|
T
|
U
|
V
|
W
|
X
|
Y-Z
G6PD Deficiency
see
glucose-6-phosphate dehydrogenase deficiency
G6PDD
see
glucose-6-phosphate dehydrogenase deficiency
GA I
see
glutaric acidemia type I
GA II
see
glutaric acidemia type II
GAA deficiency
see
Pompe disease
Galactokinase Deficiency Disease
see
galactosemia
Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease
see
galactosemia
Galactose epimerase deficiency
see
galactosemia
galactosemia
Galactosylceramidase Deficiency Disease
see
Krabbe disease
Galactosylceramide lipidosis
see
Krabbe disease
galactosylcerebrosidase deficiency
see
Krabbe disease
galactosylsphingosine lipidosis
see
Krabbe disease
GALC deficiency
see
Krabbe disease
GALT Deficiency
see
galactosemia
Gamma-hydroxybutyric acidemia
see
succinic semialdehyde dehydrogenase deficiency
gamma-hydroxybutyric aciduria
see
succinic semialdehyde dehydrogenase deficiency
Gamstorp disease
see
hyperkalemic periodic paralysis
Gamstorp episodic adynamy
see
hyperkalemic periodic paralysis
GAMT deficiency
see
guanidinoacetate methyltransferase deficiency
GAN
see
giant axonal neuropathy
Gangliosidoses GM2
Garland-Moorhouse syndrome
see
Marinesco-Sjögren syndrome
Gaucher disease
Gaucher's Disease
see
Gaucher disease
GCL
see
Krabbe disease
GD
see
Gaucher disease
GDXY
see
Swyer syndrome
Generalized Glycogenosis, Cardiac Form
see
Pompe disease
generalized lipodystrophy
see
Berardinelli-Seip congenital lipodystrophy
Genetic Brain Disorders
Genetic Diseases, X-Linked
genetic emphysema
see
alpha-1 antitrypsin deficiency
genetic hemochromatosis
see
hemochromatosis
GGM
see
glucose-galactose malabsorption
giant axonal neuropathy
Gilles de la Tourette Syndrome
see
Tourette syndrome
GLA deficiency
see
Fabry disease
Glaucoma
GLD
see
Krabbe disease
Glioblastoma, retinal
see
retinoblastoma
Glioma, retinal
see
retinoblastoma
Glucocerebrosidase deficiency
see
Gaucher disease
Glucocerebrosidosis
see
Gaucher disease
glucose-6-phosphate dehydrogenase deficiency
glucose-galactose malabsorption
glucose transport defect, blood-brain barrier
see
GLUT1 deficiency syndrome
glucose transporter protein syndrome
see
GLUT1 deficiency syndrome
glucose transporter type 1 deficiency syndrome
see
GLUT1 deficiency syndrome
Glucosyl cerebroside lipidosis
see
Gaucher disease
Glucosylceramidase deficiency
see
Gaucher disease
Glucosylceramide beta-glucosidase deficiency
see
Gaucher disease
Glucosylceramide lipidosis
see
Gaucher disease
GLUT1 deficiency syndrome
glutaric acidemia type I
glutaric acidemia type II
Glutaryl-CoA dehydrogenase deficiency
see
glutaric acidemia type I
glutathione synthetase deficiency
glyceric aciduria
see
primary hyperoxaluria
glycine encephalopathy
glycine N-methyltransferase deficiency
see
hypermethioninemia
Glycogen Storage Disease Type II
see
Pompe disease
Glycogenosis Type II
see
Pompe disease
glycolic aciduria
see
primary hyperoxaluria
glycosylasparaginase deficiency
see
aspartylglucosaminuria
GM2 Activator Deficiency Disease
see
GM2-gangliosidosis, AB variant
GM2-gangliosidosis, AB variant
GM2 gangliosidosis, type 1
see
Tay-Sachs disease
GM2 gangliosidosis, type 2
see
Sandhoff disease
GM2 Gangliosidosis, Type II
see
Sandhoff disease
GNMT deficiency
see
hypermethioninemia
Goiter-deafness syndrome
see
Pendred syndrome
Gonadal Dysgenesis, 46,XY
see
Swyer syndrome
GONADAL DYSGENESIS, XY FEMALE TYPE
see
Swyer syndrome
Gorlin syndrome
Gout
see
Lesch-Nyhan syndrome
Graefe-Usher syndrome
see
Usher syndrome
Greenfield Disease
see
metachromatic leukodystrophy
Greig cephalopolysyndactyly syndrome
Gronblad-Strandberg Syndrome
see
pseudoxanthoma elasticum
Growth Disorders
GSD II
see
Pompe disease
GTPS
see
GLUT1 deficiency syndrome
GTS
see
Tourette syndrome
guanidinoacetate methyltransferase deficiency
Gum Disease
Published: January 23, 2009