|
2631
|
|
|
Lebercilin LCA5 |
C6orf152 |
Amaurosis, Blindness, Cataract, Ciliopathies, Congenital cerebral hernia, Developmental delay, Disorder of eye, Hemiplegia/hemiparesis, Hyperopia, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Multiple congenital anomalies, Nystagmus, Retinal dystrophyView all (1 more) |
|
2632
|
|
|
Translocase of inner mitochondrial membrane 8A |
DDP, DDP1, DFN1, MTS, TIM8 |
Agammaglobulinemia, Apraxia, Attention deficit hyperactivity disorder, Central visual impairment, Dementia, Disorder of eye, Dysarthria, Dysphagia, Jensen syndrome, Mohr-tranebjaerg syndrome, Myopia, Optic atrophy, Paranoia, Sensorineural hearing loss, Sensory neuropathy |
|
2633
|
|
|
Dishevelled binding antagonist of beta catenin 2 |
C6orf116, DAPPER2, DPR2, bA503C24.7 |
|
|
2634
|
|
|
Polypeptide N-acetylgalactosaminyltransferase like 5 |
GALNACT19, GALNT15, GalNAc-T5L |
|
|
2635
|
|
|
Zinc finger protein 679 |
- |
|
|
2636
|
|
|
Polycystin 1 like 1, transient receptor potential channel interacting |
HTX8, PRO19563 |
Congenital atresia of pulmonary artery, Congenitally corrected transposition of the great arteries with ventricular septal defect, Double outlet right ventricle, Heterotaxy, visceral, Hypoplastic left heart syndrome, Paroxysmal atrial fibrillation, Right aortic arch, Situs ambiguus, Situs inversus, Transposition of great vessels, Ventricular septal defect |
|
2637
|
|
|
BMP binding endothelial regulator |
CRIM3, CV-2, CV2 |
Abnormal spinal segmentation, Alzheimer disease, Congenital clubfoot, Congenital epicanthus, Pulmonary hypoplasia, Developmental delay, Diaphanospondylodysostosis, Ischiovertebral syndrome, Liver carcinoma, Meningomyelocele, Micrognathism, Multiple renal cysts, Neck webbing, Polymicrogyria, Thoracic hypoplasia, TracheomalaciaView all (1 more) |
|
2638
|
|
|
Gasdermin E |
DFNA5, ICERE-1 |
|
|
2639
|
|
|
Zinc finger protein 800 |
- |
|
|
2640
|
|
|
Cochlin |
COCH-5B2, COCH5B2, DFNA9, DFNB110 |
|
