|
871
|
|
|
Aurora kinase B |
AIK2, AIM-1, AIM1, ARK-2, ARK2, AurB, IPL1, PPP1R48, STK-1, STK12, STK5, aurkb-sv1, aurkb-sv2 |
|
|
872
|
|
|
ATPase H+ transporting accessory protein 1 like (pseudogene) |
- |
|
|
873
|
|
|
Aminoacyl tRNA synthetase complex interacting multifunctional protein 1 |
EMAP2, EMAPII, HLD3, SCYE1, p43 |
Absence of septum pellucidum, Acquired kyphoscoliosis, Arthrogryposis multiplex congenita, Atrophy of corpus callosum, Autism, Central visual impairment, Cerebral atrophy, Congenital kyphoscoliosis, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypomyelinating leukodystrophy, Hypoplasia of corpus callosum, Mental retardation, Leukodystrophy, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Nystagmus, Pelizaeus-merzbacher disease, Polymicrogyria, Salaam seizures, Schilder disease, Seizure, Sleep disorders, Stereotyped behaviorView all (13 more) |
|
874
|
|
|
Arrestin domain containing 1 |
- |
|
|
875
|
|
|
Adhesion G protein-coupled receptor G1 |
BFPP, BPPR, CDCBM14B, CDCBM15A, GPR56, TM7LN4, TM7XN1 |
Bilateral frontoparietal polymicrogyria, Cerebellar hypoplasia, Congenital muscular dystrophy, Cortical dysplasia, Developmental delay, Dysmorphic features, Esotropia, Exotropia, Language disorders, Mental retardation, Movement disorders, Nystagmus, Pachygyria, Perisylvian polymicrogyria, Perisylvian syndrome, Polymicrogyria, Prostate cancer, Prostate cancer, hereditary, Seizure, StrabismusView all (5 more) |
|
876
|
|
|
ADAMTS like 1 |
ADAMTSL-1, ADAMTSR1, C9orf94, PUNCTIN |
Asthma, Axenfeld anomaly, Brachycephaly, Congenital glaucoma, Congenital hypothyroidism, Glaucoma, Glaucoma, congenital, Heart failure, Lung carcinoma, Macrotia, Malocclusion, Microcephaly, Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome, Migraine, Myopia, Nephrolithiasis, Parkinson disease, Retinal detachment, Rieger syndrome, Sensorineural hearing loss, Thyroid hypoplasia, Vertebrobasilar dolichoectasiaView all (7 more) |
|
877
|
|
|
Activin A receptor type 2B |
ACTRIIB, ActR-IIB, HTX4 |
Asplenia, Atrial isomerism, Ciliopathies, Dextrocardia, Ectopic spleen, Heterotaxia, Heterotaxy, visceral, Left atrial isomerism, Polysplenia, Right aortic arch, Situs ambiguus, Situs inversus, Ventricular septal defect |
|
878
|
|
|
Acid phosphatase 4 |
ACPT, AI1J |
|
|
879
|
|
|
Rho GTPase activating protein 18 |
MacGAP, SENEX, bA307O14.2 |
|
|
880
|
|
|
Adiponectin, C1Q and collagen domain containing |
ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1, GBP28 |
Adiponectin deficiency, Alveolitis, Atherosclerosis, Chromophobe carcinoma, Congestive heart failure, Coronary restenosis, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Diabetes mellitus, Diabetic nephropathy, Glomerulosclerosis, Heart failure, Hyperemia, Hyperglycemia, Hypertension, Hypoadiponectinemia, Ileocolitis, Kidney failure, Metabolic syndrome, Myocardial infarction, Myocardial ischemia, Non-alcoholic fatty liver disease, Obesity, Papillary renal carcinoma, Pulmonary fibrosis, Renal carcinoma, Rheumatoid arthritisView all (13 more) |
