|
421
|
|
|
Laminin subunit alpha 3 |
BM600, E170, JEB2A, JEB2B, JEB2C, LAMNA, LOCS |
Allergic rhinitis, Alopecia, Amelogenesis imperfecta, Amyotrophic lateral sclerosis, Anemia, Ankyloglossia, Anonychia, Aplasia cutis congenita, Cardiomyopathy, Congenital localized absence of skin, Dental enamel hypoplasia, Epidermolysis bullosa, Esophageal stricture, Hypodontia, Junctional epidermolysis bullosa, Junctional epidermolysis bullosa gravis of herlitz, Junctional split, Laryngoonychocutaneous syndrome, Laryngospasm, Laryngostenosis, Microstomia, Myocardial infarction, Nail diseases, Nail dysplasia, Nail dystrophy, Onycholysis, Osteoporosis, Ovarian neoplasm, Ovarian serous adenocarcinoma, Palmoplantar keratoderma, Paronychia inflammation, Respiratory failure, Skin carcinoma, Skin erosionView all (19 more) |
|
422
|
|
|
Laminin subunit alpha 4 |
CMD1JJ, LAMA3, LAMA4*-1 |
|
|
423
|
|
|
Laminin subunit alpha 5 |
BBDS2, NPHS26 |
|
|
424
|
|
|
Laminin subunit beta 1 |
CLM, LIS5 |
Acquired porencephaly, Agyria, Alveolitis, Autism, Cerebellar hypoplasia, Cobblestone lissencephaly, Cobblestone lissencephaly without muscular or ocular involvement, Congenital ocular coloboma, Endometrioma, Endometriosis, Hydrocephalus, Leukoencephalopathy, Lissencephaly, Macrocephaly, Mental retardation, Neuronal heterotopia, Occipital encephalocele, Pachygyria, Porencephalic cyst, Prostate cancer, Pulmonary fibrosis, Spastic paraplegia, Subcortical band heterotopia, Ulcerative colitis, Uveoretinal colobomaView all (10 more) |
|
425
|
|
|
Laminin subunit beta 2 |
LAMS, NPHS5, PIERS |
Congenital alveolar dysplasia, Cognitive disorder, Congenital clubfoot, Developmental delay, Dysphagia, Facial paralysis, High palate, Hypoplasia of iris, Hypoproteinemia, Kidney disease, Malocclusion, Mental retardation, Mesangial sclerosis, Myasthenic syndrome, Myopathy, Myopia, Nephrotic syndrome, Nephrotic syndrome with or without ocular abnormalities, Nystagmus, Pierson syndrome, Posterior lenticonus, Prostatic neoplasms, Prostate cancer, Pulmonary arterial hypertension, Scoliosis, Sleep apnea, Strabismus, Synaptic congenital myasthenic syndromes, Ventricular hypertrophyView all (14 more) |
|
426
|
|
|
Laminin subunit beta 3 |
AI1A, BM600-125KDA, JEB1A, JEB1B, LAM5, LAMNB1 |
Alopecia, Amelogenesis imperfecta, Anemia, Ankyloglossia, Anonychia, Aplasia cutis congenita, Cardiomyopathy, Colorectal cancer, Congenital localized absence of skin, Dental enamel hypoplasia, Epidermolysis bullosa, Esophageal stricture, Hypodontia, Hypoplastic amelogenesis imperfecta, Junctional epidermolysis bullosa, Junctional epidermolysis bullosa gravis of herlitz, Junctional split, Laryngospasm, Laryngostenosis, Microstomia, Nail diseases, Nail dysplasia, Nail dystrophy, Onycholysis, Osteoporosis, Palmoplantar keratoderma, Paronychia inflammation, Respiratory failure, Skin carcinoma, Skin erosionView all (15 more) |
|
427
|
|
|
Laminin subunit gamma 1 |
LAMB2 |
|
|
428
|
|
|
Lysosomal associated membrane protein 1 |
CD107a, LAMPA, LGP120 |
|
|
429
|
|
|
Laminin subunit gamma 2 |
B2T, BM600, CSF, EBR2, EBR2A, JEB3A, JEB3B, LAMB2T, LAMNB2 |
Alopecia, Amelogenesis imperfecta, Anemia, Ankyloglossia, Anonychia, Aplasia cutis congenita, Cardiomyopathy, Congenital localized absence of skin, Dental enamel hypoplasia, Epidermolysis bullosa, Epidermolysis bullosa dystrophica inversa, Esophageal stricture, Hypodontia, Junctional epidermolysis bullosa, Junctional epidermolysis bullosa gravis of herlitz, Junctional epidermolysis bullosa inversa, Junctional split, Laryngospasm, Laryngostenosis, Liver cirrhosis, Liver fibrosis, Lung carcinoma, Lupus erythematosus, Microstomia, Nail diseases, Nail dysplasia, Nail dystrophy, Onycholysis, Osteoporosis, Palmoplantar keratoderma, Paronychia inflammation, Respiratory failure, Skin carcinoma, Skin erosionView all (19 more) |
|
430
|
|
|
Lysosomal associated membrane protein 2 |
CD107b, DND, LAMP-2, LAMPB, LGP-96, LGP110 |
Amyotrophy, Cardiomyopathy, Developmental delay, Glycogen storage disease, Grand mal status epilepticus, Hypertrophic cardiomyopathy, Impaired cognition, Mental retardation, Myocardial infarction, Myocardial necrosis, Nonconvulsive status epilepticus, Petit mal status, Status epilepticus, Wolff-parkinson-white syndrome |
