941
|
|
|
ALDOA pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
942
|
|
|
ALDOA pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
943
|
|
|
Aldolase, fructose-bisphosphate B |
ALDB, ALDO2 |
Curated: Autoimmune hepatitis, Colorectal cancer, Neurodevelopmental disorder, Diabetes mellitus type 2, Hypoxia, Non-specific syndromic intellectual disability, Stomach neoplasms, hereditary fructose intolerance
Unreviewed: Adenomatous Polyposis, Anophthalmia, Basal cell nevus syndrome, Blood Coagulation Disorders, Breast neoplasm, Cataract, Cirrhosis, Colonic neoplasm, Colorectal Cancer, Colorectal neoplasm, Diabetes mellitus, Diabetes mellitus, type 2, Esophageal neoplasm, Fatty Liver, Gastric Cancer, Glioblastoma, Heart disease, Hepatocellular carcinoma, Hereditary Fructose Intolerance, Hereditary fructosuria, Hyperbilirubinemia, Hyperglycemia, Hypermagnesemia, Hyperuricemia, Hypoglycemia, Kidney Disease, Liver carcinoma, Liver Cirrhosis, Liver failure, Malnutrition, Mental retardation, Metabolic syndrome, Neoplasms, Non-Alcoholic Fatty Liver Disease, Obesity, Pancreatic neoplasm, Phosphate Diabetes, Reactive hypoglycemia, Rectal Carcinoma, Renal Carcinoma, Renal cell carcinoma, Renal Tubular Acidosis, Sclerosing cholangitis, Spherocytosis, Stomach Neoplasms, Testicular germ cell tumor, Turcot syndrome, Ulcerative colitis
|
944
|
|
|
Aldolase, fructose-bisphosphate C |
ALDC |
Curated: Autoimmune nervous system disorder
Unreviewed: Breast neoplasm, Colorectal neoplasm, Coronary artery disease, Diabetic cardiomyopathy, Diabetic retinopathy, Gallbladder neoplasm, Glioma, Melanoma, Neuroblastoma, Raynaud disease, Schizophrenia, Squamous cell carcinoma, Thyroid cancer
|
945
|
|
|
ALDOC antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
946
|
|
|
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase |
CDG1K, HMAT1, HMT-1, HMT1, MT-1, Mat-1, hMat-1 |
Curated: Congenital disorder of glycosylation, ALG1-congenital disorder of glycosylation
Unreviewed: Breast Cancer, Breast Carcinoma, Cardiomyopathy, Cerebral Atrophy, Colonic Neoplasms, Congenital Microcephaly, Developmental Delay, Diabetes Mellitus, Dysphasia, Edema, Fibroadenoma, Finnish Congenital Nephrotic Syndrome, Glycogen storage disease, Graves Disease, Hepatic Methionine Adenosyltransferase Deficiency, Hodgkin Disease, Hydrops Fetalis, Hypertrophic cardiomyopathy, Hypogonadism, Hypotonia, Impaired Cognition, Intellectual developmental disorder, Kidney Disease, Laryngeal Carcinoma, Larynx cancer, Lateral Sclerosis, Liver carcinoma, Liver failure, Lung Cancer, Lung carcinoma, Lupus Erythematosus, Lupus Nephritis, Lymphoma, Malignant Neoplasm, Microcephaly, Micrognathism, Nephritis, Nephrotic syndrome, Neurogenic Urinary Bladder, Nodular Goiter, Premature adrenarche, Proptosis, Proteinuria, Schizophrenia, Scoliosis, Seizure, Seizures, Stroke, Thyroid Diseases, Walker-Warburg Congenital Muscular Dystrophy
|
947
|
|
|
ALG10 alpha-1,2-glucosyltransferase |
ALG10A, DIE2, KCR1 |
Curated: Congenital disorder of glycosylation
Unreviewed: N/A
|
948
|
|
|
ALG10 alpha-1,2-glucosyltransferase B |
ALG10, KCR1 |
Curated: Atypical femoral fracture, Long qt syndrome, Diabetes mellitus type 2
Unreviewed: Colorectal neoplasm, Developmental and epileptic encephalopathy, Long QT Syndrome, Torsades de Pointes, Ventricular Fibrillation
|
949
|
|
|
ALG11 alpha-1,2-mannosyltransferase |
CDG1P, GT8 |
Curated: Congenital disorder of glycosylation, Crohn disease, Hepatolenticular degeneration, Inflammatory bowel disease, Ulcerative colitis, ALG11-congenital disorder of glycosylation
Unreviewed: Cerebral Atrophy, Chordoma, Congenital Microcephaly, Developmental Delay, Epilepsy, Glycogen storage disease, Hypotonia, Inborn Errors Of Metabolism, Mental retardation, Microcephaly, Neuronal Heterotopia, Psychiatric disorders, Scoliosis, Social Communication Disorder, Strabismus
|
950
|
|
|
ALG12 alpha-1,6-mannosyltransferase |
CDG1G, ECM39, PP14673, hALG12 |
Curated: Congenital disorder of glycosylation, Desbuquois syndrome, Osteoarthritis, Schizophrenia, ALG12-congenital disorder of glycosylation
Unreviewed: Cerebral palsy, Congenital Clubfoot, Congenital Hypoplasia Of Radius, Cryptorchidism, Developmental Delay, Glycogen storage disease, Hearing Loss, Hypospadias, Impaired Cognition, Patent ductus arteriosus, Patent foramen ovale, Penis Agenesis, Retinal Detachment, Retinitis Pigmentosa, Rhizomelia, Short femur
|