|
441
|
|
|
Lactate dehydrogenase C |
CT32, LDH3, LDHX |
|
|
442
|
|
|
Low density lipoprotein receptor |
FH, FHC, FHCL1, LDLCQ2 |
Amyotrophic lateral sclerosis, Aortic aneurysm, Aortic dissection, Arcus senilis, Arteriosclerosis, Atherosclerosis, Carcinoma, Cardiovascular diseases, Carotid artery disease, Cerebral artery atherosclerosis, Coronary aneurysm, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Dissection of carotid artery, Dyslipidemias, Eyelid xanthoma, Fatty liver, Homozygous hypercholesterolemia, Hypercholesterolemia, Hyperlipidemia, Hyperlipoproteinemia, Hypertension, Ischemic stroke, Lateral sclerosis, Myocardial infarction, Non-alcoholic fatty liver disease, Obesity, Peripheral arterial stenosis, Congenital hypertrophic pyloric stenosis, Q fever, Renal artery stenosis, Renal steatosis, Stroke, Supravalvar aortic stenosis, Xanthoma, Xanthoma tendinosum, XanthomatosisView all (23 more) |
|
443
|
|
|
Leukocyte cell derived chemotaxin 2 |
chm-II, chm2 |
|
|
444
|
|
|
Leptin |
LEPD, OB, OBS |
Alzheimer disease, Autism, Breast cancer, Mammary neoplasms, Breast carcinoma, Autoimmune hepatitis, Clonic seizures, Colonic neoplasms, Compensatory hyperinsulinemia, Hypoplasia of the ovary, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Diabetes mellitus, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Fatty liver, Gastric ulcer, Gynecomastia, Hypercholesterolemia, Hyperglycemia, Hyperinsulinism, Hypertension, Hypogonadism, Hypogonadotropic hypogonadism, Hypotonic seizures, Ileocolitis, Insulin-resistant diabetes mellitus, Jacksonian seizure, Leptin deficiency or dysfunction, Marfan syndrome, Mental depression, Metabolic syndrome, Non-alcoholic fatty liver disease, Nonorganic psychosis, Obesity, Oral ulcer, Sclerocystic ovaries, Penis agenesis, Physiologic amenorrhea, Polycystic ovary syndrome, Prostatic neoplasms, Prostate cancer, Psychosis, Schizophrenia, Hypothyroidism, Seizure, Senile dementia, SubfertilityView all (34 more) |
|
445
|
|
|
Leptin receptor |
CD295, LEP-R, LEPRD, OB-R, OBR |
Antibody deficiency syndrome, Asymmetric diabetic proximal motor neuropathy, Breast cancer, Mammary neoplasms, Breast carcinoma, Cirrhosis, Compensatory hyperinsulinemia, Hypoplasia of the ovary, Diabetes mellitus, Diabetic amyotrophy, Diabetic asymmetric polyneuropathy, Diabetic autonomic neuropathy, Diabetic mononeuropathy, Diabetic nephropathy, Diabetic neuralgia, Diabetic polyneuropathy, Dwarfism, Dyslipidemias, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Fatty liver, Glomerulosclerosis, Granulosa cell tumor, Gynecomastia, Hyperglycemia, Hyperinsulinism, Hyperlipidemia, Hypertension, Hypogonadism, Hypogonadotropic hypogonadism, Immunologic deficiency syndromes, Inborn errors of metabolism, Insulin-resistant diabetes mellitus, Isolated somatotropin deficiency, Kidney disease, Kidney failure, Leptin receptor deficiency, Marfan syndrome, Mood swings, Nephritis, Obesity, Pancreatic diseases, Physiologic amenorrhea, Pituitary diseases, Renal insufficiency, Hypothyroidism, Somatotropin deficiency, Subfertility, Symmetric diabetic proximal motor neuropathy, Ventricular hypertrophyView all (35 more) |
|
446
|
|
|
Leucine zipper and EF-hand containing transmembrane protein 1 |
CONDMIM, KHE, Mdm38, SLC55A1 |
Absence of septum pellucidum, Agenesis of corpus callosum, Aplasia cutis congenita, Arachnodactyly, Atrial septal defect, Axenfeld anomaly, Clonic seizures, Congenital anomaly of eye, Congenital clubfoot, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital epicanthus, Rib fusion, Congenital keratoglobus, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Frontal bossing, Congenital gallbladder anomaly, Gastroesophageal reflux disease, Hemangioma, Hypodontia, Hypoplasia of thumb, Hypospadias, Hypotonic seizures, Immunologic deficiency syndromes, Mental retardation, Jacksonian seizure, Liver carcinoma, Microcephaly, Micrognathism, Microtia, Movement disorders, Multicystic renal dysplasia, Hypotonia, Nystagmus, Optic atrophy, Osteoporosis, Otitis media, Pitt-rogers-danks syndrome, Polydactyly, Precocious puberty, Primary tethered cord syndrome, Proptosis, Ptosis, Radioulnar synostosis, Retinal diseases, Rieger syndrome, Sclerocornea, Scoliosis, Seizure, Situs inversus, Stenosis of external auditory canal, Stereotyped behavior, Strabismus, Ventricular septal defect, Wolf-hirschhorn syndromeView all (43 more) |
|
447
|
|
|
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase |
SCDO3 |
Abnormal spinal segmentation, Congenital diaphragmatic hernia, Congenital exomphalos, Rib fusion, Congenital meningocele, Cryptorchidism, Dwarfism, Hypospadias, Jarcho-levin syndrome, Macrocephaly, Mental retardation, Microcephaly, Pulmonary venous return anomaly, Scoliosis, Spina bifida occulta, Spondylocostal dysostosis, Syndactyly of fingersView all (2 more) |
|
448
|
|
|
Galectin 1 |
GAL1, GBP |
|
|
449
|
|
|
Galectin 2 |
HL14 |
|
|
450
|
|
|
Galectin 3 |
CBP35, GAL3, GALBP, GALIG, L31, LGALS2, MAC2 |
|
