|
71
|
|
|
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) |
|
72
|
|
|
Protein phosphatase 1 regulatory subunit 13 like |
ARCME, CMAEA, IASPP, NKIP1, RAI, RAI4 |
|
|
73
|
|
|
Progesterone receptor membrane component 1 |
Dap1, HPR6.6, IZA, MPR |
|
|
74
|
|
|
Prokineticin receptor 1 |
GPR73, GPR73a, PK-R1, PKR1, ZAQ |
|
|
75
|
|
|
PPARG coactivator 1 alpha |
LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A, PPARGC1 |
Amyotrophic lateral sclerosis, Anxiety disorder, Bowen`s disease, Congestive heart failure, Diabetes mellitus, Heart failure, Impaired cognition, Laryngospasm, Lewy body disease, Mental depression, Mood swings, Myocardial infarction, Neuronal ceroid lipofuscinosis, Parkinson disease, Respiratory failure, SchizophreniaView all (1 more) |
|
76
|
|
|
Patatin like domain 6, lysophospholipase |
BNHS, LNMS, NTE, NTEMND, OMCS, SPG39, iPLA2delta, sws |
Accessory nipple, Alopecia, Anterior horn cell disease, Spinocerebellar ataxia, Ataxia-hypogonadism-choroidal dystrophy syndrome, Atrophy of the spinal cord, Brachycephaly, Brachydactyly, Camptodactyly of fingers, Cataract, Cerebellar ataxia-hypogonadism syndrome, Cerebellar atrophy, Charcot-marie-tooth disease, Chorioretinal dystrophy, Chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism, Congenital coloboma of iris, Congenital epicanthus, Congenital hepatic fibrosis, Congenital hypoplasia of penis, Cryptorchidism, Dementia, Diabetes mellitus, Distal amyotrophy, Dwarfism, Dysarthria, Gordon holmes syndrome, Gynecomastia, Hearing loss, Hemiplegia/hemiparesis, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Lateral sclerosis, Laurence-moon syndrome, Limb muscle atrophy, Mental retardation, Motor neuron disease, Nervous system diseases, Nervous system disorder, Nystagmus, Obesity, Oliver-mcfarlane syndrome, Optic atrophy, Penis agenesis, Peripheral axonal neuropathy, Polydactyly, Polyneuropathy, Renal insufficiency, Retinal dystrophy, Retinitis pigmentosa, Sick building syndrome, Somatotropin deficiency, Spastic paraplegia, Speech disorders, Strabismus, Syndactyly of fingers, Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, Hereditary spastic paraplegia, x-linkedView all (42 more) |
|
77
|
|
|
Poly(A) polymerase alpha |
PAP, PAP-alpha |
|
|
78
|
|
|
Peroxiredoxin 3 |
AOP-1, AOP1, HBC189, MER5, PPPCD, PRO1748, SCAR32, SP-22, prx-III |
|
|
79
|
|
|
POP1 ribonuclease P/MRP subunit |
ANXD2 |
|
|
80
|
|
|
PITX2 adjacent non-coding RNA |
- |
|
