|
841
|
|
|
ADAM metallopeptidase domain 7 |
ADAM 7, ADAM-7, EAPI, GP-83, GP83 |
|
|
842
|
|
|
Actinin alpha 2 |
CMD1AA, CMH23, CMYO8, CMYP8, MPD6, MYOCOZ |
|
|
843
|
|
|
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 |
AMAP2, CENTB3, DDEF2, PAG3, PAP, Pap-alpha, SHAG1 |
|
|
844
|
|
|
Aldehyde dehydrogenase 1 family member A2 |
DIH4, RALDH(II), RALDH2, RALDH2-T |
Alzheimer disease, Arthritis, Atrial fibrillation, Barrett esophagus, Cardiovascular diseases, Coronary heart disease, Diabetes, Diabetes mellitus, Digestive system disorders, Esophageal cancer, Exudative macular degeneration, Gastrointestinal diseases, Geographic atrophy, Gout, Gouty arthritis, Heart failure, Intestinal diseases, Ischemic stroke, Age-related macular degeneration, Malignant neoplasm, Meningomyelocele, Metabolic syndrome, Myelocele, Osteoarthrosis deformans, Parkinson disease, Parkinsonian disease, Prostatic neoplasms, Prostate cancer, Ramsay hunt paralysis syndrome, Schizophrenia, StrokeView all (16 more) |
|
845
|
|
|
Apelin |
APEL, XNPEP2 |
|
|
846
|
|
|
Actinin alpha 3 |
ACTN3D |
|
|
847
|
|
|
Adaptor related protein complex 1 subunit sigma 2 |
DC22, MRX59, MRXS21, MRXS5, MRXSF, PGS, SIGMA1B |
Autism, Cerebral cortical atrophy, Choreoathetosis, Cryptorchidism, Developmental delay, Dwarfism, Fried syndrome, Hearing loss, High palate, Hydrocephalus, Mental retardation, Intellectual disability-dandy-walker malformation-basal ganglia disease-seizures syndrome, x-linked, Intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome, x-linked, Spastic diplegia, Macrocephaly, Macrostomia, Macrotia, Malocclusion, Microcephaly, Myopathy, Pettigrew syndrome, Scoliosis, StrabismusView all (8 more) |
|
848
|
|
|
Adaptor related protein complex 1 subunit mu 1 |
AP47, CLAPM2, CLTNM, MU-1A, mu1A |
|
|
849
|
|
|
- |
- |
Wolff-parkinson-white syndrome, Ataxia and polyneuropathy, Basal ganglia cysts, Bicuspid aortic valve, Cardiomyopathy, Cardiomyopathy, apical hypertrophic and neuropathy, Cerebral cortical atrophy, Charcot-marie-tooth disease, Choreoathetosis, Cleft palate and bilateral cleft lip, Dementia, Demyelinating neuropathy, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyskinetic syndrome, Dysphagia, Gastroesophageal reflux disease, Hearing loss, Hereditary leber optic atrophy, Histiocytoid cardiomyopathy, Horizontal pendular nystagmus, Hypertrophic cardiomyopathy, Mental retardation, Isolated atp synthase deficiency, Leigh syndrome, Liver failure, Maternally inherited leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial diseases, Mitochondrial myopathy, Mitochondrial spastic paraplegia, Myoclonic seizures, Myopathy, Myopathy, lactic acidosis, and sideroblastic anemia, Nervous system diseases, Neuropathy ataxia and retinis pigmentosa, Nystagmus, Optic atrophy, Periodic paralysis with distal motor neuropathy, Peripheral axonal neuropathy, Polyneuropathy, Retinal diseases, Retinal telangiectasia, Retinitis pigmentosa, Rod-cone dystrophy, Seizure, Sensorimotor neuropathy, Sensory neuropathy, Spastic tetraparesis, Striatonigral degeneration, Postaxial hand polydactyly, Ventricular preexcitation, West syndromeView all (42 more) |
|
850
|
|
|
- |
- |
Bicuspid aortic valve, Cardiomyopathy, Cardiomyopathy, apical hypertrophic and neuropathy, Complete atrioventricular block, Hemiplegia/hemiparesis, Histiocytoid cardiomyopathy, Hypopituitarism, Isolated atp synthase deficiency, Kearns sayre syndrome, Optic neuropathy, Periodic paralysis with distal motor neuropathy, Progressive external ophthalmoplegia |
