|
41
|
|
|
Origin recognition complex subunit 6 |
ORC6L |
Bronchomalacia, Camptodactyly of fingers, Breast aplasia, Anotia, Mandibular aplasia, Congenital clubfoot, Breast hypoplasia, Congenital hypoplasia of penis, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Ear diseases, Ear-patella-short stature syndrome, Epispadias, Gastroesophageal reflux disease, Hypertrophy of clitoris, Hypoplasia of the maxilla, Hypospadias, Laryngomalacia, Meier-gorlin syndrome, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Myeloproliferative disorder, Penis agenesis, Posteriorly rotated ear, Respiratory failure, Seckel syndrome, Specific learning disorder, Submucosal cleft palate, TracheomalaciaView all (19 more) |
|
42
|
|
|
Olfactomedin like 2B |
- |
|
|
43
|
|
|
Oxysterol binding protein like 3 |
ORP-3, ORP3, OSBP3 |
|
|
44
|
|
|
Opsin 1, medium wave sensitive |
CBBM, CBD, COD5, GCP, GOP, OPN1MW1 |
Achromatopsia incomplete, x-linked, Blue cone monochromacy, Bornholm eye disease, Color blindness, Cone dysfunction syndrome with myopia, x-linked, Cone dystrophy, x-linked, Cone monochromatism, Cone-rod dystrophy, Corneal dystrophy, Deuteranomaly, Myopia, Nyctalopia, Nystagmus, Partial color blindness, Pendular nystagmus |
|
45
|
|
|
Orofacial cleft 1 candidate 1 (pseudogene) |
MRDS1, Opo |
|
|
46
|
|
|
Olfactory receptor family 1 subfamily J member 2 |
HG152, HSA5, OR1J3, OR1J5, OR9-19, OST044 |
|
|
47
|
|
|
5-oxoprolinase, ATP-hydrolysing |
5-Opase, OPLA, OPLAHD |
|
|
48
|
|
|
Olfactory receptor family 51 subfamily B member 5 |
HOR5'Beta5, OR11-37 |
|
|
49
|
|
|
Olfactory receptor family 5 subfamily J member 2 |
OR11-266 |
|
|
50
|
|
|
Olfactory receptor family 4 subfamily C member 13 |
- |
|
