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331
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ATP binding cassette subfamily A member 4 |
ABC10, ABCR, ARMD2, CORD3, FFM, RMP, RP19, STGD, STGD1 |
Retinopathy, Atrophic retina, Retinitis pigmentosa, Blindness, Breast cancer, Central nervous system cancer, Kidney disease, Colorectal neoplasm, Cone dystrophy, Cone-rod dystrophy, Glioblastoma, Glioma, Heart failure, Macular degeneration, Leber congenital amaurosis, Macular dystrophy, Mandibulofacial dysostosis, Night blindness, congenital stationary, Optic atrophy, Orofacial cleft, Ovarian cancer, Peripheral neuropathy, Retinal detachment, Retinopathy background, Stargardt disease, Vitreoretinal degenerationView all (11 more) |
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332
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|
|
Arachidonate 5-lipoxygenase |
5-LO, 5-LOX, 5LPG, LOG5 |
Arteriosclerosis, Rheumatoid arthritis, Asthma, Atherosclerosis, Renal cell carcinoma, Colitis, Colonic neoplasm, Hyperalgesia, Pulmonary hypertension, Metabolic syndrome, Nephrosclerosis, Oligodendroglioma, Ovarian neoplasm, Pancreatic neoplasm, Prostatic neoplasm, Stomach neoplasms, Tuberculosis, Diabetes mellitus, type 2, UrticariaView all (4 more) |
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333
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|
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Arachidonate 5-lipoxygenase activating protein |
FLAP |
Asthma, Atherosclerosis, Bipolar disorder, Brain infarction, Ischemic stroke, Cerebral palsy, Ischemic heart disease, Coronary artery disease, Crohn disease, Inflammatory bowel disease, Kidney disease, Liver disease, Myocardial infarction, Myocardial ischemia, Proteinuria, Ulcerative colitisView all (1 more) |
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334
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Arachidonate 12-lipoxygenase, 12R type |
12R-LOX, ARCI2 |
Autism, Congenital ichthyosis, Renal cell carcinoma, Colonic neoplasm, Congenital nonbullous ichthyosiform erythroderma, Ichthyosis, Lamellar ichthyosis, Ovarian neoplasm, Pancreatic neoplasm, Prostatic neoplasm, Uterine polyp |
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335
|
|
|
Arachidonate 12-lipoxygenase pseudogene 2 |
ALOX12E |
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336
|
|
|
ATPase H+ transporting V0 subunit d2 |
ATP6D2, VMA6 |
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337
|
|
|
Arachidonate 15-lipoxygenase |
12-LOX, 15-LOX, 15-LOX-1, LOG15 |
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338
|
|
|
AFG1 like ATPase |
AFG1, LACE1, c222389 |
|
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339
|
|
|
Alkaline phosphatase, biomineralization associated |
AP-TNAP, APTNAP, HOPS, HPPA, HPPC, HPPI, HPPO, TNALP, TNAP, TNS-ALP, TNSALP |
Hypophosphatasia, Alzheimer disease, Aortic stenosis, Aortic valve disease, Bladder calculus, Bone disease, Bone fragility with contractures, arterial rupture, and deafness, Calcinosis, Childhood hypophosphatasia, Connective tissue disease, Desbuquois syndrome, Hyperparathyroidism, Liver disease, Metabolic bone disorder, Micromelia, Nephrolithiasis, Osteoarthritis, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome, Seizures, Ureterolithiasis, UrolithiasisView all (7 more) |
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340
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ABL proto-oncogene 1, non-receptor tyrosine kinase |
ABL, BCR-ABL, CHDSKM, JTK7, bcr/abl, c-ABL, c-ABL1, p150, v-abl |
B-lymphoblastic leukemia/lymphoma, Bone disease, Breast neoplasm, Carcinogenesis, Myelogenous leukemia, Myeloid leukemia, Colorectal cancer, Congenital contractural arachnodactyly, Congenital heart defects, Congenital heart disease, Congenital hemihypertrophy, Connective tissue disease, Developmental disability, Esophageal neoplasm, Congenital heart defect, Liver neoplasm, Moyamoya angiopathyView all (2 more) |