|
511
|
|
|
LDL receptor related protein 6 |
ADCAD2, EVR8, STHAG7 |
Anodontia, Clinodactyly, Coronary artery disease, Diabetes mellitus, Gout, Hypercholesterolemia, Hypertension, Hypodontia, Hypoplasia of the maxilla, Metabolic syndrome, Microdontia, Micrognathism, Myocardial infarction, Oligodontia, Osteoporosis, Tooth agenesis, Triple negative breast neoplasmsView all (2 more) |
|
512
|
|
|
LDL receptor related protein 5 |
BMND1, EVR1, EVR4, HBM, LR3, LRP-5, LRP-7, LRP7, OPPG, OPS, OPTA1, PCLD4, VBCH2 |
Acquired kyphoscoliosis, Angle closure glaucoma, Brachycephaly, Cataract, Congenital blindness, Congenital kyphoscoliosis, Congenital nystagmus, Congenital retinal fold, Craniosynostosis, Developmental delay, Disorder of eye, Dwarfism, Endosteal hyperostosis, Exudative retinopathy, Exudative vitreoretinopathy, Facial paralysis, Frontal bossing, Gastroesophageal reflux disease, Glioma, Hearing loss, Horizontal pendular nystagmus, Hyperostosis, Hyperostosis of skull, Polycystic liver disease, Liver cyst, Macrocephaly, Malocclusion, Mental retardation, Microcephaly, Microphthalmos, Multiple congenital anomalies, Multiple renal cysts, Nystagmus, Optic atrophy, Osteopenia, Osteopetrosis, Osteoporosis, Osteoporosis-pseudoglioma syndrome, Osteosclerosis, Osteosclerosis-developmental delay-craniosynostosis syndrome, Phthisis bulbi, Polycystic liver disease with kidney cysts, Proliferative vitreoretinopathy, Renal cyst, Retinal detachment, Retinopathy, Subcapsular cataract, Van buchem disease, Ventricular septal defect, Vitreoretinal degeneration, Worth diseaseView all (36 more) |
|
513
|
|
|
LDL receptor related protein associated protein 1 |
A2MRAP, A2RAP, HBP44, MRAP, MYP23, RAP, alpha-2-MRAP |
|
|
514
|
|
|
Limbic system associated membrane protein |
IGLON3, LAMP |
|
|
515
|
|
|
Lymphocyte specific protein 1 |
WP34, pp52 |
|
|
516
|
|
|
Lanosterol synthase |
APMR4, CTRCT44, HYPT14, OSC |
Alopecia, Alopecia-mental retardation syndrome, Cataract, Congenital cataract, Developmental delay, Hypotrichosis, Hypotrichosis simplex, Lipoidosis, Mental retardation, Microcephaly, Q fever |
|
517
|
|
|
Leukotriene A4 hydrolase |
- |
|
|
518
|
|
|
Lymphotoxin alpha |
LT, TNFB, TNFSF1, TNLG1E |
Cervix carcinoma, Coronary arteriosclerosis, Coronary artery disease, Diabetes mellitus, Esophagus neoplasm, Fulminant hepatic failure with cerebral edema, Hepatic coma, Hepatic encephalopathy, Hepatic stupor, Leprosy, Lupus erythematosus, Malignant mesothelioma, Myocardial infarction, Psoriatic arthritis, Schizophrenia, SepticemiaView all (1 more) |
|
519
|
|
|
Latent transforming growth factor beta binding protein 1 |
ARCL2E |
|
|
520
|
|
|
Latent transforming growth factor beta binding protein 2 |
C14orf141, GLC3D, LTBP3, MSPKA, MSTP031, WMS3 |
Alzheimer disease, Aortic valve sclerosis, Brachydactyly, Cataract, Congenital glaucoma, Congenital keratoglobus, Dwarfism, Ectopia lentis, Exfoliation syndrome, Glaucoma, Glaucoma secondary to spherophakia/ectopia lentis and megalocornea, Glaucoma, congenital, Hypoplasia of thumb, Marfan syndrome, Mental retardation, Microspherophakia, Microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma, Myocardial infarction, Myopia, Ocular hypertension, Phakomatosis pigmentovascularis, Pulmonary stenosis, Retinal detachment, Ventricular septal defect, Weill-marchesani syndromeView all (10 more) |
