6351
|
|
|
Inositol polyphosphate-5-phosphatase E |
CORS1, CPD4, JBTS1, MORMS, PPI5PIV, pharbin |
Basal cell carcinoma, Lung disease, Ciliary dyskinesia, Coach syndrome, Congenital brain malformation, Congenital clubfoot, Congenital hemivertebra, Congenital hypoplasia of femur, Congenital hypoplasia of part of brain, Cutaneous squamous cell carcinoma, Eye disease, Aplasia of the vermis, Hydranencephaly, Inflammatory bowel disease, Intellectual developmental disorder, Joubert syndrome, Leber congenital amaurosis, Lissencephaly, Macrogyria, Micrognathism, Microgyria, Obesity, Optic atrophy, Patent ductus arteriosus, Penile disease, Retinitis pigmentosa, Rod-cone dystrophy, Skeletal dysplasia, UranostaphyloschisisView all (14 more) |
6352
|
|
|
Inositol polyphosphate-5-phosphatase F |
MSTP007, MSTPO47, SAC2, hSAC2 |
|
6353
|
|
|
Inositol polyphosphate-5-phosphatase K |
MDCCAID, PPS, SKIP |
|
6354
|
|
|
Inositol polyphosphate phosphatase like 1 |
OPSMD, SHIP2 |
|
6355
|
|
|
Insulin |
IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10, PNDM4 |
22q13.3 deletion syndrome, Alzheimer disease, Bipolar disorder, Cardiac arrest, Cardiomyopathy, Congestive heart failure, Cystic kidney disease, Delirium, dementia, and cognitive disorders, Bipolar depression, Diabetes mellitus type 1, Diabetes mellitus, Diabetes mellitus ketosis prone, Diabetes mellitus type 2, Permanent neonatal diabetes mellitus, Diabetic cardiomyopathy, Diabetic ketoacidosis, Diabetic neuropathy, Diabetic retinopathy, Dystonia, dopa-responsive, with or without hyperphenylalaninemia, Edema, Fatty liver, Fatty liver, alcoholic, Gout, Heart failure, Hyperglycemia, Hyperinsulinism, Hyperkalemia, Hyperproinsulinemia, Hypertension, Hypertriglyceridemia, Hypertrophic cardiomyopathy, Hypoglycemia, Hypotension, Idiopathic diabetes, Kidney disease, Kidney failure, Latent autoimmune diabetes in adults, Lewy body disease, Liver disease, Liver failure, Maturity-onset diabetes of the young (mody), Memory disorders, Metabolic syndrome, Maturity-onset diabetes of the young, Myopathy, Neonatal diabetes mellitus, Neural tube defect, Neural tube defects, x-linked, Nonalcoholic fatty liver disease, Obesity, Pancreatitis, Panic disorder, Paralysis, Paresthesia, Parkinson disease, Polycystic ovary syndrome, Potassium deficiency, Prostatic neoplasms, Rhabdomyolysis, Seizures, 22q13 monosomy syndrome, Transient neonatal diabetes mellitus, Depression, Urinary bladder diseases, Ventricular dysfunction, Ventricular fibrillation, Ventricular outflow obstructionView all (52 more) |
6356
|
|
|
INS-IGF2 readthrough |
INSIGF |
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Beckwith-wiedemann syndrome, Hepatocellular carcinoma, Celiac disease, Cervical cancer, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Permanent neonatal diabetes mellitus, Diabetic cardiomyopathy, Diabetic ketoacidosis, Gout, Hyperglycemia, Hyperproinsulinemia, Hypoglycemia, Juvenile idiopathic arthritis, Latent autoimmune diabetes in adults, Maturity-onset diabetes of the young (mody), Major depressive disorder, Neonatal diabetes mellitus, Psoriasis, Silver-russell syndrome, Systemic lupus erythematosus, Ulcerative colitisView all (13 more) |
6357
|
|
|
INSC spindle orientation adaptor protein |
- |
|
6358
|
|
|
Insulin induced gene 1 |
CL6 |
|
6359
|
|
|
Insulin induced gene 2 |
INSIG-2 |
|
6360
|
|
|
Insulin like 3 |
RLF, RLNL, ley-I-L |
|
