|
201
|
|
|
GLI family zinc finger 3 |
ACLS, GCPS, GLI3-190, GLI3FL, PAP-A, PAPA, PAPA1, PAPB, PHS, PPDIV |
Acrania, Acrocallosal syndrome, Addison`s disease, Adrenocorticotropic hormone deficiency, Agenesis of corpus callosum, Ambiguous genitalia, Anencephaly, Aortic coarctation, Aplasia cutis congenita, Arrhinencephaly, Atrial septal defect, Brachydactyly, Cerebellar hypoplasia, Choanal atresia, Colorectal cancer, Tibial hemimelia, Congenital clubfoot, Congenital diaphragmatic hernia, Congenital exomphalos, Rib fusion, Congenital heart defects, Pulmonary hypoplasia, Congenital pectus carinatum, Craniorachischisis, Craniosynostosis, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Diaphragmatic eventration, Diastematomyelia, Distal arthrogryposis, Dwarfism, Ectopic kidney, Epilepsy, Foot polydactyly, Frontal bossing, Gastric cancer, Gastrointestinal stromal tumor, Glioma, Gonadotropin deficiency, Greig cephalopolysyndactyly syndrome, Growth hormone deficiency, Hearing loss, Holoprosencephaly, Hydrocephalus, Hydrometrocolpos, Hydronephrosis, Hypogonadism, Hypopigmentation disorder, Hypopituitarism, Hypoplasia of the epiglottis, Hypospadias, Hypothalamic hamartomas, Imperforate anus, Mental retardation, Isolated somatotropin deficiency, Laryngeal cleft, Leukemia, Macrocephaly, Meningomyelocele, Microglossia, Micrognathism, Micromelia, Microphthalmos, Microtia, Nail diseases, Nail dysplasia, Neural tube defect, Neurenteric cyst, Occipital encephalocele, Oligodactyly, Osteochondrodysplasia, Osteochondroma, Pallister-hall syndrome, Panhypopituitarism, Patent ductus arteriosus, Penis agenesis, Polydactyly, Polydactyly of fingers, Polysyndactyly, Postaxial polydactyly, Precocious puberty, Biliary cirrhosis, Primary tethered cord syndrome, Ptosis, Radial polydactyly, Renal agenesis, Renal aplasia, Renal cyst, Renal dysplasia, Renal hypoplasia, Scaphocephaly, Scoliosis, Adrenal insufficiency, Hypothyroidism, Skeletal dysplasia, Somatotropin deficiency, Spinal cord myelodysplasia, Split hand foot deformity, Stomach neoplasms, Supernumerary metacarpal bone, Syndactyly of fingers, Syndactyly of the toes, Talipes, Tarsal coalition, Thyroid dysgenesis, Thyroid hypoplasia, Trigonocephaly, Postaxial hand polydactyly, Ventricular septal defectView all (95 more) |
|
202
|
|
|
Glyoxalase I |
GLOD1, GLYI, HEL-S-74 |
|
|
203
|
|
|
Glucagon like peptide 1 receptor |
GLP-1, GLP-1-R, GLP-1R |
|
|
204
|
|
|
Glycine receptor alpha 1 |
HKPX1, STHE |
Congenital exomphalos, Developmental delay, Dyssomnia, Dystonia, Eosinophilia, Focal dystonia, Gastroesophageal reflux disease, Hereditary hyperekplexia, Hiatal hernia, Hyperekplexia, Mental retardation, Nocturnal epilepsy, Pycnodysostosis, Sleep disorders, Writer`s cramp |
|
205
|
|
|
Glycine receptor alpha 2 |
GLR, MRXSP |
|
|
206
|
|
|
Glycine receptor beta |
HKPX2 |
Astigmatism, Congenital exomphalos, Dyssomnia, Eosinophilia, Esotropia, Gastroesophageal reflux disease, Hereditary hyperekplexia, Hiatal hernia, Hyperekplexia, Mental retardation, Myopia, Sleep disorders |
|
207
|
|
|
Glutaminase |
AAD20, CASGID, DEE71, EIEE71, GAC, GAM, GDPAG, GLS1, KGA |
Arthritis, Cerebellar ataxia, Developmental delay, Epileptic encephalopathy, Febrile seizures, Hyperkeratosis, Miscarriage, Hypotonia, Osteoarthrosis deformans, Respiratory failure, Spastic ataxia-dysarthria |
|
208
|
|
|
Glutamate dehydrogenase 1 |
GDH, GDH1, GLUD, hGDH1 |
Attention deficit hyperactivity disorder, Compensatory hyperinsulinemia, Hyperinsulinemic hypoglycemia, Developmental delay, Endogenous hyperinsulinism, Epilepsy, Exogenous hyperinsulinism, Hyperinsulinism, Hyperinsulinism-hyperammonemia syndrome, Hypoglycemic coma, Hypoglycemic seizures, Mental retardation, Reactive hypoglycemia, Specific learning disorder |
|
209
|
|
|
Glutamate dehydrogenase 2 |
GDH2, GLUDP1 |
|
|
210
|
|
|
Glutamate-ammonia ligase |
DEE116, GLNS, GS, PIG43, PIG59 |
Brain atrophy, Central nervous system inborn metabolic diseases, Cerebral atrophy, Congenital brain dysgenesis due to glutamine synthetase deficiency, Epileptic encephalopathy, Fulminant hepatic failure with cerebral edema, Hepatic coma, Hepatic encephalopathy, Hepatic stupor, Hypoplasia of corpus callosum, Liver carcinoma, Mental depression, Mood disorder, Obesity, Psychosis, SchizophreniaView all (1 more) |
