|
1221
|
|
|
Chorionic gonadotropin subunit beta 3 |
CGB, CGB5, CGB7, CGB8, LHB, hCGB |
|
|
1222
|
|
|
DIAPH2 antisense RNA 1 |
EPAG |
|
|
1223
|
|
|
Fatty acid hydroxylase domain containing 2 |
C5orf4 |
|
|
1224
|
|
|
Aldehyde dehydrogenase 1 family member L1 |
10-FTHFDH, 10-fTHF, FDH, FTHFD |
|
|
1225
|
|
|
Formimidoyltransferase cyclodeaminase |
LCHC1 |
|
|
1226
|
|
|
Protein phosphatase 1 regulatory subunit 17 |
C7orf16, GSBS |
|
|
1227
|
|
|
Caseinolytic mitochondrial matrix peptidase chaperone subunit X |
EPP2 |
|
|
1228
|
|
|
Phosphodiesterase 10A |
ADSD2, HSPDE10A, IOLOD, LINC00473, PDE10A19 |
Anxiety disorder, Benign chorea with striatal involvement, Bipolar disorder, Cardiovascular diseases, Conduct disorder, Developmental delay, Dysarthria, Dyskinesia, limb and orofacial, Dyskinetic syndrome, Generalized dyskinesia with orofacial involvement, Hemiballismus, Hyperthyroidism, Hypothyroidism, Orofacial dyskinesia, Mental retardation, Motor delay, Nonorganic psychosis, Parkinson disease, Psychosis, Striatal degenerationView all (5 more) |
|
1229
|
|
|
Snf2 related CREBBP activator protein |
DEHMBA, DOMO1, EAF1, FLHS, SWR1 |
Adenocarcinoma, Brachydactyly, Camptodactyly of fingers, Celiac disease, Short clavicles, Congenital hypoplasia of penis, Congenital posterior urethral valves, Developmental delay, Dwarfism, Dysmorphic features, Exotropia, Facial wart, Floating-harbor syndrome, Hyperopia, Hyperopic astigmatism, Macrostomia, Macrotia, Malabsorption syndrome, Mental retardation, Micrognathism, Microstomia, Multiple congenital anomalies, Multiple myeloma, Neurodevelopmental disorders, Nystagmus, Oral aversion, Oral cleft, Otitis media, Penile hypospadias, Persistent pupillary membranes, Posteriorly rotated ear, Sleep apnea, Speech disorders, Strabismus, Submucosal cleft palate, TrigonocephalyView all (21 more) |
|
1230
|
|
|
Protein phosphatase 1 regulatory subunit 13 like |
ARCME, CMAEA, IASPP, NKIP1, RAI, RAI4 |
|
