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631
|
|
|
Leucine zipper like post translational regulator 1 |
BTBD29, LZTR-1, NS10, NS2, SWNTS2 |
Abnormal dermatoglyphic pattern, Aortic coarctation, Asthma, Autism, Brachydactyly, Camptodactyly of fingers, Cardiofaciocutaneous syndrome, Congenital pectus carinatum, Congenital pectus excavatum, Costello syndrome, Cryptorchidism, Developmental delay, Dwarfism, Dysarthria, Dysmorphic features, Giant cell glioblastoma, Glioblastoma, Gliosarcoma, Hearing loss, Heart septal defects, High palate, Hydrops fetalis, Hypogonadotropic hypogonadism, Leopard syndrome, Cystic hygroma, Melanocytic nevus, Mental retardation, Micrognathism, Mitral valve stenosis, Myocardial infarction, Neck webbing, Neurilemmoma, Neurofibromatosis, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Nystagmus, Posteriorly rotated ear, Proptosis, Ptosis, Pulmonary artery dilatation, Pulmonary stenosis, Radioulnar synostosis, Schwannomatosis, Scoliosis, Spinal cord neoplasms, StrabismusView all (31 more) |
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632
|
|
|
L antigen family member 3 |
CVG5, DXS9879E, DXS9951E, ESO3, GAMOS2, ITBA2, Pcc1 |
Aqueductal stenosis, Arachnodactyly, Cerebellar atrophy, Cerebral atrophy, Developmental delay, Dwarfism, Esotropia, Galloway-mowat syndrome, Glomerulonephritis, Glomerulosclerosis, Hemiplegia/hemiparesis, Hiatal hernia, High palate, Impaired cognition, Kidney disease, Macrotia, Mental retardation, Microcephaly, Micrognathism, Nephrotic syndrome, Nystagmus, Pachygyria, Polymicrogyria, ScoliosisView all (9 more) |
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633
|
|
|
L3MBTL histone methyl-lysine binding protein 2 |
H-l(3)mbt-l, L3MBT |
|
|
634
|
|
|
Leucine rich melanocyte differentiation associated |
C10orf11, CDA017 |
Albinism, Alopecia, Alopecia, male pattern, Androgenetic alopecia, Atrial fibrillation, Chronic obstructive pulmonary disease, Diabetes mellitus, Disorder of eye, Nystagmus, Oculocutaneous albinism, Paroxysmal atrial fibrillation, Scleroderma |
|
635
|
|
|
Lysyl oxidase like 4 |
LOXC |
|
|
636
|
|
|
Latent transforming growth factor beta binding protein 4 |
ARCL1C, LTBP-4, LTBP4L, LTBP4S |
Bladder diverticulum, Bronchomalacia, Cardiomyopathy, Congenital exomphalos, Pulmonary hypoplasia, Cutis laxa, Cutis laxa with pulmonary, gastrointestinal and urinary anomalies, Developmental delay, Duchenne muscular dystrophy, Gastroesophageal reflux disease, Giant cell glioblastoma, Glioblastoma, Hydronephrosis, Impaired cognition, Laryngomalacia, Lung diseases, Micrognathism, Motor delay, Patent foramen ovale, Rectal prolapse, Scoliosis, Specific learning disorder, TracheomalaciaView all (8 more) |
|
637
|
|
|
Leucine zipper tumor suppressor 2 |
LAPSER1 |
|
|
638
|
|
|
L3MBTL histone methyl-lysine binding protein 3 |
MBT-1, MBT1 |
|
|
639
|
|
|
Ligand dependent nuclear receptor corepressor |
C10orf12, MLR2 |
|
|
640
|
|
|
Late cornified envelope 3D |
LEP16, SPRL6A, SPRL6B |
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