|
111
|
|
|
O-sialoglycoprotein endopeptidase |
GAMOS3, GCPL1, KAE1, OSGEP1, PRSMG1, TCS3 |
Aqueductal stenosis, Arachnodactyly, Cerebellar atrophy, Cerebral atrophy, Congenital camptodactyly, Congenital epicanthus, Developmental delay, Dwarfism, Dysmorphic features, Galloway-mowat syndrome, Glomerulonephritis, Glomerulosclerosis, Hemiplegia/hemiparesis, Hiatal hernia, High palate, Hypertension, Hypoalbuminemia, Hypoplasia of corpus callosum, Impaired cognition, Kidney disease, Macrotia, Mental retardation, Mesangial sclerosis, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Nephrotic syndrome, Pachygyria, StrabismusView all (15 more) |
|
112
|
|
|
Olfactomedin like 3 |
HNOEL-iso, OLF44 |
|
|
113
|
|
|
OTU deubiquitinase 7B |
CEZANNE, ZA20D1 |
|
|
114
|
|
|
- |
- |
|
|
115
|
|
|
Ovo like zinc finger 2 |
CHED, CHED1, CHED2, EUROIMAGE566589, PPCD1, ZNF339 |
Cerebellar ataxia, Cerebellar atrophy, Congenital hereditary endothelial dystrophy, Corneal dystrophy, Corneal endothelial dystrophy, Ectropion uveae, Excessive tearing, Glaucoma, Mitochondrial dna deletion syndrome, Pilomatrixoma, Polymorphous corneal dystrophy, Synechiae |
|
116
|
|
|
Oligosaccharyltransferase complex non-catalytic subunit |
DC2 |
|
|
117
|
|
|
Opsin 1, long wave sensitive |
CBBM, CBP, COD5, RCP, ROP |
Achromatopsia incomplete, x-linked, Blue cone monochromacy, Bornholm eye disease, Color blindness, Cone dysfunction syndrome with myopia, x-linked, Cone monochromatism, Cone-rod dystrophy, Corneal dystrophy, Myopia, Nyctalopia, Nystagmus, Partial color blindness, Pendular nystagmus, Protanomaly |
|
118
|
|
|
Opsin 1, short wave sensitive |
BCP, BOP, CBT |
|
|
119
|
|
|
Oligosaccharyltransferase complex subunit pseudogene 2 |
- |
|
|
120
|
|
|
Otoconin 90 |
PLA2L |
|
