|
461
|
|
|
DNA ligase 4 |
LIG4S |
Alopecia, Amyloidosis, Anemia, Asthma, Attention deficit hyperactivity disorder, Blepharophimosis, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Combined immunodeficiency, Congenital epicanthus, Congenital hypoplasia of penis, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Cutis marmorata, Developmental delay, Diabetes mellitus, Dubowitz syndrome, Dwarfism, Dysmorphic features, Eczema, Eosinophilia, Exfoliative dermatitis, High palate, Hydrocephalus, Hydronephrosis, Hypoparathyroidism, Hypospadias, Hypothyroidism, Leukemia, Lig4 syndrome, Lymphocytic leukemia, Lymphoma, Lymphoblastic leukemia, Lymphopenia, Macrostomia, Malabsorption syndrome, Mental retardation, Microcephaly, Micrognathism, Multiple myeloma, Myelodysplasia, Myelodysplastic syndrome, Myeloproliferative disorder, Myopia, Nephrotic syndrome, Nystagmus, Omenn syndrome, Pancytopenia, Papillary thyroid carcinoma, Paraproteinemia, Penis agenesis, Pituitary dwarfism, Psoriasiform eczema, Ptosis, Rectal prolapse, Scoliosis, Seckel syndrome, Severe combined immunodeficiency disease, Spina bifida occulta, Strabismus, Submucosal cleft palate, Syndactyly of the toes, ThyroiditisView all (51 more) |
|
462
|
|
|
Lens intrinsic membrane protein 2 |
CTRCT19, MP17, MP19 |
|
|
463
|
|
|
LIM domain kinase 1 |
LIMK, LIMK-1 |
Abnormal dermatoglyphic pattern, Abnormal spinal segmentation, Accessory kidney, Aneurysm of aortic arch, Anxiety disorder, Arnold-chiari malformation, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Camptodactyly of fingers, Cataract, Cerebral cortical atrophy, Cholelithiasis, Congenital anomaly of neck, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of penis, Congenital keratoglobus, Congenital pectus excavatum, Congestive heart failure, Cornea plana, Cryptorchidism, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dysgraphia, Gastroesophageal reflux disease, Glaucoma, Hearing loss, Hypercalcemia, Hypertension, Hypertrophic cardiomyopathy, Hypodontia, Hypogonadotropic hypogonadism, Hypothyroidism, Macroglossia, Macrostomia, Macrotia, Malabsorption syndrome, Mental depression, Mental retardation, Microcephaly, Microdontia, Micrognathism, Mitral valve prolapse, Multiple renal cysts, Myocardial infarction, Myopathy, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus-induced head nodding, Obesity, Obsessive-compulsive disorder, Osteopenia, Osteoporosis, Osteosclerosis, Otitis media, Overriding aorta, Patent ductus arteriosus, Pelvic kidney, Peptic ulcer, Peripheral pulmonary artery stenosis, Phakomatosis pigmentovascularis, Polycystic ovary syndrome, Posterior embryotoxon, Precocious puberty, Pulmonary stenosis, Radioulnar synostosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Scoliosis, Spina bifida occulta, Strabismus, Stroke, Supravalvar aortic stenosis, Tetralogy of fallot, Ventricular septal defect, Vesicoureteral reflux, Williams syndromeView all (70 more) |
|
464
|
|
|
LIM domain kinase 2 |
- |
|
|
465
|
|
|
Lipase A, lysosomal acid type |
CESD, LAL |
Adrenal calcification, Anemia, Arteriosclerosis, Cholestasis, Cholesterol ester storage disease, Cirrhosis, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Developmental delay, Esophageal varix, Fatty liver, Hydrops fetalis, Hypercholesterolemia, Liver failure, Liver fibrosis, Malnutrition, Myocardial infarction, Niemann-pick disease, Pulmonary arterial hypertension, Sphingomyelinase deficiency, Wolman diseaseView all (7 more) |
|
466
|
|
|
Lipase C, hepatic type |
HDLCQ12, HL, HTGL, LIPH |
Atrial fibrillation, Cardiovascular diseases, Coronary heart disease, Diabetes, Diabetes mellitus, Exudative macular degeneration, Geographic atrophy, Heart failure, Hepatic lipase deficiency, Hypercholesterolemia, Hyperemia, Hyperlipidemia, Hyperlipoproteinemia, Lipid metabolism, inborn errors, Age-related macular degeneration, Malignant neoplasm, Metabolic syndrome, Schizophrenia, Stroke, XanthomaView all (5 more) |
|
467
|
|
|
Lipase E, hormone sensitive type |
AOMS4, FPLD6, HSL, LHS, REH |
|
|
468
|
|
|
LLGL scribble cell polarity complex component 2 |
HGL, Hugl-2, LGL2 |
|
|
469
|
|
|
LLGL scribble cell polarity complex component 1 |
DLG4, HUGL, HUGL-1, HUGL1, LLGL, Lgl1, Mgl1 |
|
|
470
|
|
|
Long intergenic non-protein coding RNA 200 |
C10orf139, NCRNA00200 |
|
