|
471
|
|
|
Long intergenic non-protein coding RNA 2649 |
- |
|
|
472
|
|
|
Long intergenic non-protein coding RNA 2656 |
- |
|
|
473
|
|
|
Lectin, mannose binding 1 |
ERGIC-53, ERGIC53, F5F8D, FMFD1, MCFD1, MR60, gp58 |
|
|
474
|
|
|
LBX1 antisense RNA 1 |
MUSE |
|
|
475
|
|
|
Lamin A/C |
CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 |
Absent eyebrow, Acanthosis nigricans, Acquired kyphoscoliosis, Acrosteolysis, Adrenal hypoplasia, x-linked, Alopecia, Amyotrophy, Anomalous pulmonary artery, Aortic valve calcification, Aortic valve sclerosis, Arrhythmogenic right ventricular cardiomyopathy, Arteriosclerosis, Arthritis, Arthrogryposis multiplex congenita, Atherosclerosis, Atrial fibrillation, Atrial septal defect, Atrioventricular block, Blepharophimosis, Brachydactyly, Bradyarrhythmia, Mammary neoplasms, Carcinoid tumor of lung, Carcinoma, Cardiac conduction disease, Cardiocutaneous progeria syndrome, Cardiomyopathy, Carotid artery stenosis, Cataract, Charcot-marie-tooth disease, Choanal atresia, Chondrocalcinosis, Clinodactyly, Breast aplasia, Congenital myopathy with fiber type disproportion, Congenital deformity of foot, Congenital anomaly of the hand, Short clavicles, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital muscular dystrophy, Congenital pectus excavatum, Congestive heart failure, Coronary arteriosclerosis, Cranial nerve paralysis, Defect of skull ossification, Developmental delay, Dextrocardia, Diabetes mellitus, Dilated cardiomyopathy with conduction defect, Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome, Distal amyotrophy, Distal lower limb amyotrophy, Double ureter, Dwarfism, Dysautonomia, Eclampsia, Elbow flexion contracture, Emery-dreifuss muscular dystrophy, Emery-dreifuss muscular dystrophy, x-linked, Entropion, Fatty liver, Focal segmental glomerulosclerosis, Glomerulosclerosis, Hearing loss, Heart block, Heart-hand syndrome, High palate, Hutchinson-gilford syndrome, Hydropic placenta, Hypercholesterolemia, Hyperglycemia, Hyperinsulinism, Hyperkeratosis, Hyperlipidemia, Hyperopia, Hyperphosphatemia, Hypertension, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadism, Hypogonadotropic hypogonadism, Hypohidrosis, Hypoplasia of nipple, Hypoplasia of teeth, Hypospadias, Hypotrichosis, Ichthyosis, Insulin-resistant diabetes mellitus, Intervertebral disc degeneration, Intestinal neoplasms, Ischemic myocardial dysfunction, Keratoconjunctivitis sicca, Kidney neoplasm, Laryngomalacia, Left ventricular hypertrophy, Left ventricular noncompaction, Lethal tight skin contracture syndrome, Limb-girdle muscle atrophy, Limb-girdle muscular dystrophy, Benign scapuloperoneal muscular dystrophy with cardiomyopathy, Linear scleroderma, Lipoatrophy, Lipodystrophic laminopathy, Lipodystrophy, Scleroderma, Lung neoplasms, Lung adenocarcinoma, Macrotia, Malouf syndrome, Mandibuloacral dysostosis, Mandibuloacral dysplasia with lipodystrophy, Meningioma, Microcolon, Micrognathism, Microstomia, Mitral valve prolapse, Monogenic diabetes, Morphea, Motor delay, Mouth neoplasms, Muscular dystrophy, Myocardial infarction, Myopathy, Nail diseases, Nail dysplasia, Najjar syndrome, Neck webbing, Hypotonia, Neuromuscular diseases, Obesity, Osteopenia, Osteoporosis, Osteosarcoma, Ovarian neoplasm, Sclerocystic ovaries, Pancreatitis, Papillary renal carcinoma, Parkinson disease, Partial lipodystrophy, Patchy hypo- and hyperpigmentation, Patent ductus arteriosus, Pericardial effusion, Peripheral arterial stenosis, Peripheral axonal atrophy, Peripheral neuropathy, Peroneal muscle atrophy, Poikiloderma, Polycystic ovary syndrome, Precocious puberty, Premature menopause, Progeria, Proptosis, Ptosis, Renal glomerular disease, Restrictive dermopathy, Rheumatoid arthritis, Sclerosis of hand bone, Scoliosis, Secondary physiologic amenorrhea, Sinoatrial block, Sinus tachycardia, Skin neoplasms, Skin carcinoma, Skin erosion, Sprengel deformity, Subcutaneous calcification, Submucosal cleft palate, Supraventricular tachycardia, Syndactyly, Talipes, Temporomandibular ankylosis, Thrombocytosis, Thyroid neoplasm, Transient ischemic attack, Transposition of great vessels, Ventricular arrhythmia, Ventricular cardiomyopathy, Ventricular hypertrophy, Ventricular tachycardia, Vertical talus, Vocal cord paralysis, Werner syndrome, XanthomatosisView all (169 more) |
|
476
|
|
|
Long intergenic non-protein coding RNA 2389 |
- |
|
|
477
|
|
|
Lamin B1 |
ADLD, ADLDAT, LMN, LMN2, LMNB, MCPH26 |
Atrophy of corpus callosum, Atrophy of the spinal cord, Cerebral cortical atrophy, Cockayne syndrome, Demyelinating leukodystrophy, Developmental delay, Dysarthria, Dysautonomia, Dysphagia, Erectile dysfunction, Hypohidrosis, Hypomyelinating leukodystrophy, Leukodystrophy, Lung adenocarcinoma, Mental depression, Mental retardation, Nystagmus, Pelizaeus-merzbacher disease, Pseudobulbar palsyView all (4 more) |
|
478
|
|
|
Long intergenic non-protein coding RNA 2694 |
C15orf53 |
|
|
479
|
|
|
LIM domain only 1 |
RBTN1, RHOM1, TTG1 |
|
|
480
|
|
|
LIM domain only 2 |
LMO-2, RBTN2, RBTNL1, RHOM2, TTG2 |
|
