|
91
|
|
|
Opioid receptor mu 1 |
LMOR, M-OR-1, MOP, MOR, MOR1, OPRM |
Ballismus, Clonic seizures, Dyskinetic syndrome, Epilepsy, Fulminant hepatic failure with cerebral edema, Hemiballismus, Hepatic coma, Hepatic encephalopathy, Hepatic stupor, Hypotonic seizures, Jacksonian seizure, Lymphocytic leukemia, Orofacial dyskinesia, Mental depression, Mood disorder, Movement disorders, Nonorganic psychosis, Oral dyskinesia, Psychosis, Respiratory failure, Schizophrenia, Seizure, Status marmoratusView all (8 more) |
|
92
|
|
|
Origin recognition complex subunit 1 |
HSORC1, ORC1L, PARC1 |
Blepharophimosis, Camptodactyly of fingers, Breast aplasia, Anotia, Mandibular aplasia, Congenital camptodactyly, Congenital clubfoot, Breast hypoplasia, Congenital hypoplasia of penis, Congenital microcephaly, Congenital pectus carinatum, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Ear diseases, Ear-patella-short stature syndrome, Epispadias, Frontal bossing, Gastroesophageal reflux disease, High palate, Hypertrophy of clitoris, Hypoplasia of the maxilla, Hypospadias, Liver carcinoma, Meier-gorlin syndrome, Mental retardation, Microcephaly, Microdontia, Micrognathism, Microlissencephaly, Microstomia, Microtia, Myeloproliferative disorder, Osteochondritis dissecans, Penis agenesis, Posteriorly rotated ear, Respiratory failure, Seckel syndrome, Specific learning disorder, Strabismus, Submucosal cleft palate, Syndactyly of fingersView all (28 more) |
|
93
|
|
|
Origin recognition complex subunit 4 |
ORC4L, ORC4P |
Bronchomalacia, Camptodactyly of fingers, Breast aplasia, Anotia, Mandibular aplasia, Congenital camptodactyly, Breast hypoplasia, Congenital hypoplasia of penis, Craniosynostosis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Ear diseases, Ear-patella-short stature syndrome, Epispadias, Gastroesophageal reflux disease, Gout, Gouty arthritis, Hypertrophy of clitoris, Hypoplasia of the maxilla, Hypospadias, Meier-gorlin syndrome, Mental retardation, Microcephaly, Micrognathism, Microstomia, Microtia, Myeloproliferative disorder, Posteriorly rotated ear, Respiratory failure, Seckel syndrome, Specific learning disorder, Submucosal cleft palate, TracheomalaciaView all (20 more) |
|
94
|
|
|
Orosomucoid 1 |
A1AG1, AGP-A, AGP1, HEL-S-153w, ORM |
|
|
95
|
|
|
Oxysterol binding protein |
OSBP1 |
|
|
96
|
|
|
Oncostatin M |
- |
|
|
97
|
|
|
Ornithine transcarbamylase |
OCTD, OTC1, OTCD, OTCase |
|
|
98
|
|
|
Orthodenticle homeobox 2 |
CPHD6, MCOPS5 |
Agenesis of corpus callosum, Agnathia-holoprosencephaly-situs inversus syndrome, Anxiety disorder, Autism, Bipolar disorder, Macular dystrophy, patterned, Cataract, Mandibular aplasia, Congenital hypoplasia of penis, Congenital ocular coloboma, Cryptorchidism, Cyclocephaly, Developmental delay, Diabetes insipidus, Disorder of eye, Dwarfism, Dysgnathia complex, Dysmorphic features, Dyssomnia, Ectopic anterior pituitary gland, Esophageal atresia, Hearing loss, Hemiplegia/hemiparesis, Holoprosencephaly, Horizontal nystagmus, Hypoglycemia, Hypogonadotropic hypogonadism, Hypohidrosis, Hypoplasia of the optic nerve, Isolated microphthalmia-anophthalmia-coloboma, Jaw abnormalities, Kallmann syndrome, Medulloblastoma, Medullomyoblastoma, Mental retardation, Microcornea, Microglossia, Microphthalmia, Syndromic microphthalmia, Microphthalmos, Microstomia, Microtia, Multiple congenital anomalies, Nystagmus, Obesity, Osteopenia, Osteoporosis of vertebrae, Otocephaly, Panhypopituitarism, Pituitary dwarfism, Pituitary hormone deficiency, Polydactyly, Retinal dystrophy, Hypothyroidism, Septo-optic dysplasia, Situs inversus, Sleep disorders, Strabismus, SynotusView all (44 more) |
|
99
|
|
|
Oviductal glycoprotein 1 |
CHIT5, EGP, MUC9, OGP |
|
|
100
|
|
|
Ovo like transcriptional repressor 1 |
HOVO1 |
|
