|
171
|
|
|
Growth hormone releasing hormone receptor |
GHRFR, GRFR, IGHD1B, IGHD4 |
|
|
172
|
|
|
Growth hormone secretagogue receptor |
GHDP, GHS-R1a, GHSR-1a |
Digestive system neoplasms, Dwarfism, Dysmorphic features, Gastric cancer, Hypoglycemia, Isolated somatotropin deficiency, Ketosis, Short stature, idiopathic, autosomal, Somatotropin deficiency |
|
173
|
|
|
Gastric inhibitory polypeptide |
- |
|
|
174
|
|
|
Gastric inhibitory polypeptide receptor |
PGQTL2 |
|
|
175
|
|
|
Gap junction protein alpha 1 |
AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL, HLHS1, HSS, ODDD, PPKCA |
Cubitus valgus, Adenoma, Alopecia, Palmoplantar keratoderma and congenital alopecia, Anhedonia, Atrial septal defect, Atrioventricular block, Atrioventricular septal defect, Autism, Basaran yilmaz syndrome, Blepharophimosis, Brachycephaly, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Camptodactyly of fingers, Cataract, Clinodactyly, Complete atrioventricular canal defect, Congenital alopecia totalis, Congenital epicanthus, Congenital exomphalos, Hypoplastic aortic arch, Congestive heart failure, Coronary aneurysm, Craniometaphyseal dysplasia, Dental enamel hypoplasia, Diabetes mellitus, Dwarfism, Dysarthria, Dysmorphic features, Erythrokeratoderma, Erythrokeratodermia variabilis, Erythrokeratodermia variabilis et progressiva, Facial paralysis, Fifth finger distal phalanx clinodactyly, Fingernail dysplasia, Frontal bossing, Glaucoma, Hallermann`s syndrome, Hearing loss, Hypertension, Hypoglycemia, Hypoplasia of teeth, Hypoplasia of the maxilla, Hypoplastic left heart syndrome, Hypotrichosis, Keratosis pilaris, Lung neoplasms, Lung cancer, Macrocephaly, Madelung deformity, Malocclusion, Marfan syndrome, Mental depression, Mental retardation, Microcephaly, Microcornea, Microdontia, Micrognathism, Microphthalmos, Microstomia, Mitral valve stenosis, Movement disorders, Multiple congenital anomalies, Myopia, Nail diseases, Nail dysplasia, Neurogenic urinary bladder, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Nystagmus, Oculodentodigital dysplasia, Optic atrophy, Osteochondrodysplasia, Osteopetrosis, Palmoplantar keratoderma, Palmoplantar keratosis, Papillary adenoma, Partial atrioventricular canal defect, Patchy palmoplantar keratoderma, Patent ductus arteriosus, Persistent pupillary membranes, Polydactyly, Prostatic neoplasms, Prostate cancer, Pulmonary arterial hypertension, Pyle metaphyseal dysplasia, Respiratory tract diseases, Skeletal dysplasia, Skin cancer, Skin neoplasms, Strabismus, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Taurodontism, Ventricular septal defectView all (84 more) |
|
176
|
|
|
G protein-coupled receptor 160 |
GPCR1, GPCR150 |
|
|
177
|
|
|
Gap junction protein alpha 3 |
CTRCT14, CX46, CZP3 |
|
|
178
|
|
|
Gap junction protein alpha 4 |
CX37 |
|
|
179
|
|
|
Gap junction protein alpha 5 |
ATFB11, CX40 |
Aortic coarctation, Atrial cardiomyopathy, Atrial fibrillation, Atrial standstill, Atrioventricular block, Autism, Bicuspid aortic valve, Brachydactyly, Camptodactyly of fingers, Cryptorchidism, Dolichocephaly, Endocardial fibroelastosis, Frontal bossing, Hypertension, Mental retardation, Microcephaly, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Persistent truncus arteriosus, Proptosis, Schizophrenia, Tetralogy of fallot, Transposition of great vesselsView all (8 more) |
|
180
|
|
|
Gap junction protein alpha 8 |
CAE, CAE1, CTRCT1, CX50, CZP1, MP70 |
Aortic coarctation, Autism, Bicuspid aortic valve, Capsular cataract, Cataract, Cataract-microcornea syndrome, Congenital cataract, Congenital coloboma of iris, Corneal dystrophy, Frontal bossing, Mental retardation, Microcephaly, Microcornea, Multiple congenital anomalies, Myopia, Nystagmus, Patent ductus arteriosus, Persistent truncus arteriosus, Pulverulent cataract, Schizophrenia, Sclerocornea, Transposition of great vesselsView all (7 more) |
