|
451
|
|
|
Receptor like tyrosine kinase |
D3S3195, JTK5, JTK5A, RYK1 |
|
|
452
|
|
|
Ryanodine receptor 1 |
CCO, CMYO1A, CMYO1B, CMYP1A, CMYP1B, KDS, MHS, MHS1, PPP1R137, RYDR, RYR, RYR-1, SKRR |
Acquired kyphoscoliosis, Amyotrophy, Arthrogryposis multiplex congenita, Autism, Benign samaritan congenital myopathy, Blood coagulation disorders, Congenital alveolar dysplasia, Bulbar palsy, Cardiomyopathy, Central core disease, Centronuclear myopathy, Centronuclear myopathy, x-linked, Chromophobe carcinoma, Cleidocranial dysplasia, Congenital clubfoot, Congenital contracture, Developmental dysplasia of the hip, Congenital epicanthus, Congenital myopathy with fiber type disproportion, Pulmonary hypoplasia, Congenital kyphoscoliosis, Congenital multicore myopathy with external ophthalmoplegia, Congenital muscular dystrophy, Congenital myopathy, Congenital myopathy with myasthenic-like onset, Congenital neuromuscular disease, Congenital structural myopathy, Congestive heart failure, Cryptorchidism, Developmental delay, Distal arthrogryposis, Dolichocephaly, Dysarthria, Dysmorphic features, Dysphagia, External ophthalmoplegia, Facial paralysis, Hemangioma, cavernous, High palate, Hip contracture, Hydrops fetalis, Hyperphosphatemia, King denborough syndrome, Left ventricular hypertrophy, Lethal multiple pterygium syndrome, Liver failure, Mental retardation, Microstomia, Minicore myopathy with external ophthalmoplegia, Mitral valve prolapse, Multiminicore disease with hand involvement, Motor delay, Movement disorders, Multiminicore disease, Multiple pterygium syndrome, Muscular dystrophy, Myasthenia gravis, Myopathy, Necrotizing myopathy, Hypotonia, Neuromuscular diseases, Papillary renal carcinoma, Pena shokeir syndrome, Penis agenesis, Peripheral axonal neuropathy, Plagiocephaly, Postnatal asphyxia, Ptosis, Rectus femoris muscle atrophy, Renal carcinoma, Respiratory failure, Sacral agenesis, Scoliosis, Sternocleidomastoid amyotrophy, Supraventricular tachycardia, Tubular aggregate myopathy, Ventricular tachycardiaView all (62 more) |
|
453
|
|
|
Ryanodine receptor 2 |
ARVC2, ARVD2, RYR-2, RyR, VACRDS, VTSIP |
Arrhythmogenic right ventricular cardiomyopathy, Autism spectrum disorder, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Diabetic cardiomyopathy, Hypertrophic cardiomyopathy, Long qt syndrome, Malignant mesothelioma, Myocardial ischemia, Narcolepsy, Paroxysmal ventricular fibrillation, Schizophrenia, Stress-induced polymorphic ventricular tachycardia, Ventricular arrhythmia, Ventricular cardiomyopathy, Ventricular fibrillation, Ventricular tachycardiaView all (2 more) |
|
454
|
|
|
Ryanodine receptor 3 |
CMYO20, CMYP20, RYR-3 |
|
|
455
|
|
|
Ring finger protein 123 |
FP1477, KPC1 |
|
|
456
|
|
|
RNA binding motif protein 26 |
ARRS2, C13orf10, PPP1R132, PRO1777, SE70-2, ZC3H17 |
|
|
457
|
|
|
Ribokinase |
RBSK, RK |
|
|
458
|
|
|
Ras related GTP binding C |
GTR2, LNGODS, LNGOS, RAGC, TIB929 |
|
|
459
|
|
|
Rabenosyn, RAB effector |
KAREVS, MFANDO, Rabenosyn-5, ZFYVE20 |
|
|
460
|
|
|
Roundabout guidance receptor 3 |
HGPPS, HGPPS1, HGPS, RBIG1, RIG1 |
Autism, Cerebellar hypoplasia, Gaze palsy, familial horizontal, with progressive scoliosis, Gaze palsy, with progressive scoliosis, Hearing loss, Horizontal gaze palsy with progressive scoliosis, Impaired cognition, Nystagmus, Ophthalmoplegia, Scoliosis, Supranuclear gaze palsy, Thoracolumbar scoliosis |
