201
|
|
|
Inositol polyphosphate-5-phosphatase D |
SHIP, SHIP-1, SHIP1, SIP-145, hp51CN, p150Ship |
|
202
|
|
|
Inositol polyphosphate phosphatase like 1 |
OPSMD, SHIP2 |
Brachydactyly, Congenital pectus excavatum, Cryptorchidism, Diabetes mellitus, Dolichocephaly, Dwarfism, Frontal bossing, Hypertension, Macrocephaly, Metabolic syndrome, Micromelia, Opsismodysplasia, Rhizomelia, Schneckenbecken dysplasia, Scoliosis, StrokeView all (1 more) |
203
|
|
|
Insulin induced gene 1 |
CL6 |
|
204
|
|
|
Insulin like 3 |
RLF, RLNL, ley-I-L |
|
205
|
|
|
INSM transcriptional repressor 1 |
IA-1, IA1 |
|
206
|
|
|
Insulin receptor |
CD220, HHF5 |
Acanthosis nigricans, Alzheimer disease, Asymmetric diabetic proximal motor neuropathy, Brachydactyly, Cardiovascular diseases, Cholestasis, Compensatory hyperinsulinemia, Congenital diaphragmatic hernia, Congenital exomphalos, Posterolateral diaphragmatic hernia, Morgagni diaphragmatic hernia, Hyperinsulinemic hypoglycemia, Cryptorchidism, Developmental delay, Diabetes mellitus, Diabetes mellitus with acanthosis nigricans, Diabetic amyotrophy, Diabetic asymmetric polyneuropathy, Diabetic autonomic neuropathy, Diabetic ketoacidosis, Diabetic mononeuropathy, Diabetic nephropathy, Diabetic neuralgia, Diabetic polyneuropathy, Dwarfism, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Female pseudohermaphroditism, Gastric cancer, Gout, Gouty arthritis, Gynecomastia, High palate, Hyperglycemia, Hyperinsulinism, Hyperkeratosis, Hypertrichosis, Hypertrophy of clitoris, Hypertrophy of nail, Hypoglycemia, Hypoglycemic coma, Hypoglycemic seizures, Hypothyroidism, Impaired cognition, Insulin resistance syndrome, Insulin-resistant diabetes mellitus, Leprechaunism syndrome, Lewy body disease, Lipoatrophy, Lipodystrophy, Liver fibrosis, Lung diseases, Macrostomia, Macrotia, Malocclusion, Microcephaly, Monogenic diabetes, Nail diseases, Nail dysplasia, Nervous system diseases, Onychogryposis, Ovarian cysts, Parkinson disease, Polycystic ovary syndrome, Precocious puberty, Proptosis, Rabson-mendenhall syndrome, Renal carcinoma, Senile dementia, Symmetric diabetic proximal motor neuropathyView all (55 more) |
207
|
|
|
Insulin receptor related receptor |
IRR |
|
208
|
|
|
Intracisternal A particle-promoted polypeptide |
KLHL27 |
|
209
|
|
|
Imprinted in Prader-Willi syndrome |
NCRNA00002 |
Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorderView all (7 more) |
210
|
|
|
Interleukin 1 receptor associated kinase 1 |
IRAK, pelle |
Alopecia, Anorexia, Anoxic-ischemic encephalopathy, Arthritis, Cerebral hypoxia-ischemia, Coronary arteriosclerosis, Coronary artery disease, Glioblastoma, Hypoxic-ischemic encephalopathy, Impaired cognition, Ischemic encephalopathy, Language disorders, Lung adenocarcinoma, Lupus anticoagulant, Lupus erythematosus, Lymphopenia, Microangiopathic hemolytic anemia, Myositis, Nephritis, Nephrotic syndrome, Oral ulcer, Pericardial effusion, Pleural effusion, Psychosis, Raynaud phenomenon, Renal insufficiency, Rheumatoid arthritis, Syndromic mental retardation, x-linked, Systemic lupus erythematosusView all (14 more) |