501
|
|
|
Long intergenic non-protein coding RNA 2908 |
C9orf139 |
|
502
|
|
|
Lysyl oxidase like 1 |
LOL, LOXL |
Urinary bladder cancer, Bladder neoplasm, Cataract, Diverticular diseases, Exfoliation syndrome, Glaucoma, Lens subluxation, Liver cirrhosis, Liver fibrosis, Phacodonesis, Retinal vein occlusion |
503
|
|
|
Lysyl oxidase like 2 |
LOR, LOR2, WS9-14 |
|
504
|
|
|
Lipoprotein(a) |
AK38, APOA, LP |
Aortic valve calcification, Atherosclerosis, Carcinoma, Cardiovascular diseases, Congenital lipoprotein deficiency, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Coronary syndrome, Diabetes, Diabetes mellitus, Hypercholesterolemia, Hypoprebetalipoproteinemia, Liver carcinoma, Myocardial infarction, Rheumatic aortic stenosis, Stroke, Thrombosis, Vascular diseasesView all (4 more) |
505
|
|
|
Lipoprotein lipase |
HDLCQ11, LIPD |
Anaplastic carcinoma, Apolipoprotein c2 deficiency, Carcinoma, Cardiomyopathy, Cardiovascular diseases, Celiac disease, Colonic neoplasms, Coronary artery disease, Coronary heart disease, Diabetes mellitus, Dyslipidemias, Hypercholesterolemia, Hyperlipidemia, Hyperlipoproteinemia, Hypertension, Lipidemia retinalis, Lipoprotein lipase deficiency, Metabolic syndrome, Myocardial diseases, Myocardial infarction, Obesity, Pancreatitis, Prostatic neoplasms, Prostate cancer, Schizophrenia, Vascular diseases, XanthomaView all (12 more) |
506
|
|
|
Lactoperoxidase |
SPO |
|
507
|
|
|
LIM domain containing preferred translocation partner in lipoma |
- |
Allergic rhinitis, Allergic sensitization, Alopecia areata, Arthritis, Asthma, Autoimmune diseases, Autoimmune thyroiditis, B-cell neoplasm, Basal cell neoplasm, Carcinoma, Celiac disease, Classical hodgkin lymphoma, Crohn disease, Eczema, Glaucoma, Graves disease, Hashimoto disease, Hodgkin disease, Hypothyroidism, Immune system diseases, Inflammatory bowel disease, Juvenile arthritis, Kidney failure, Lymphocytic leukemia, Leukemia, Lupus erythematosus, Multiple myeloma, Multiple sclerosis, Myeloid leukemia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Respiratory tract diseases, Skin carcinoma, Still disease, VitiligoView all (20 more) |
508
|
|
|
LDL receptor related protein 1 |
A2MR, APOER, APR, CD91, DDH3, IGFBP-3R, IGFBP3R, IGFBP3R1, KPA, LRP, LRP1A, TGFBR5 |
Abdominal migraine, Aortic aneurysm, Atrophoderma vermiculata, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Comedone, Common migraine, Confusional migraine, Coronary artery disease, Excessive tearing, Hemicrania migraine, Keratosis follicularis spinulosa decalvans, Keratosis pilaris, Mental depression, Migraine, Moyamoya disease, Schizophrenia, Status migrainosus, Ulerythema ophryogenesisView all (6 more) |
509
|
|
|
LDL receptor related protein 2 |
DBS, GP330, LRP-2 |
Colorectal cancer, Congenital coloboma of iris, Congenital diaphragmatic hernia, Congenital exomphalos, Congenital malrotation of intestine, Congenital omphalocele, Development disorder, Developmental delay, Diaphragmatic eventration, Donnai-barrow syndrome, Eye diseases, Hearing loss, Hyperuricemia, Kidney disease, Kidney failure, Macrocephaly, Mental retardation, Metabolic bone disorder, Multiple sclerosis, Myopia, Non-acidotic proximal tubulopathy, Osteopenia, Partial agenesis of corpus callosum, Posteriorly rotated ear, Prolactinoma, Proptosis, Prostatic neoplasms, Prostate cancer, Acute kidney insufficiency, Retinal detachment, Retinal dystrophy, Schizophrenia, Ventricular septal defect, Vitamin d deficiencyView all (19 more) |
510
|
|
|
LDL receptor related protein 4 |
CLSS, CMS17, LRP-4, LRP10, MEGF7, SOST2 |
Abnormal dermatoglyphic pattern, Cataract, Cenani-lenz syndrome, Congenital anomaly of nose, Congenital hypoplasia of radius, Myasthenic syndrome, Developmental delay, Ectropion, Facial paralysis, Fingernail dysplasia, Frontal bossing, Hearing loss, High palate, Hypodontia, Hypoplasia of thumb, Hypothyroidism, Laryngomalacia, Macrocephaly, Malocclusion, Micrognathism, Micromelia, Nail diseases, Nail dysplasia, Nystagmus, Odontome, Optic atrophy, Osteosclerosis, Polydactyly, Polysyndactyly, Proptosis, Ptosis, Radioulnar synostosis, Renal agenesis, Renal hypoplasia, Respiratory failure, Schizophrenia, Sclerosteosis, Scoliosis, Syndactyly, Syndactyly of fingers, Syndactyly of the toesView all (26 more) |