|
521
|
|
|
Plexin A2 |
OCT, PLXN2 |
|
|
522
|
|
|
Protein kinase AMP-activated non-catalytic subunit gamma 3 |
AMPKG3, SMGMQTL |
|
|
523
|
|
|
PTOV1 extended AT-hook containing adaptor protein |
ACID2, PTOV-1 |
|
|
524
|
|
|
Plexin B1 |
PLEXIN-B1, PLXN5, SEP |
|
|
525
|
|
|
Phorbol-12-myristate-13-acetate-induced protein 1 |
APR, NOXA |
|
|
526
|
|
|
Pro-melanin concentrating hormone |
MCH, ppMCH |
|
|
527
|
|
|
Prepronociceptin |
N/OFQ, NOP, OFQ, PPNOC, ppN/OFQ |
|
|
528
|
|
|
PML nuclear body scaffold |
MYL, PP8675, RNF71, TRIM19 |
Anemia, Anorexia, Diffuse alveolar hemorrhage, Disseminated intravascular coagulation, Exfoliation syndrome, Fibrinogen deficiency, Gangrene, Giant cell glioblastoma, Glioblastoma, Hypofibrinogenemia, Leukopenia, Myocardial infarction, Myopia, Neutropenia, Paget disease, Pancytopenia, Promyelocytic leukemia, Prostatic neoplasms, Prostate cancer, Schizophrenia, Stevens-johnson syndrome, Stomatitis, Treatment related secondary malignancyView all (8 more) |
|
529
|
|
|
Phosphomannomutase 2 |
CDG1, CDG1a, CDGS, PMI, PMI1, PMM 2 |
Acquired kyphoscoliosis, Antithrombin deficiency, Cardiomyopathy, Cataract, Cerebellar hypoplasia, Cerebral atrophy, Cerebral palsy, Coloboma of optic disc, Colorectal cancer, Colorectal neoplasms, Aplasia of the ovary, Congenital diaphragmatic hernia, Congenital disorder of glycosylation, Congenital epicanthus, Congenital kyphoscoliosis, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Diabetes mellitus, Dysmorphic features, Esotropia, Fatty liver, Glaucoma, High palate, Hydrops fetalis, Hyperinsulinism, Hypertension, Hypertrophic cardiomyopathy, Hypoalbuminemia, Hypocholesterolemia, Hypogonadism, Hypogonadotropic hypogonadism, Hypoplasia of nipple, Hypothyroidism, Mental retardation, Lipodystrophy, Liver fibrosis, Macrostomia, Macrotia, Malocclusion, Microcephaly, Movement disorders, Multiple renal cysts, Muscular dystrophy, Myopia, Nephrotic syndrome, Nervous system diseases, Nystagmus, Osteopenia, Osteoporosis, Pericardial effusion, Pericarditis, Periventricular leukomalacia, Pleural effusion, Polycystic kidney disease, Polyneuropathy, Premature menopause, Pulmonary stenosis, Renal cyst, Rod-cone dystrophy, Strabismus, Synophrys, Thrombocytosis, Thrombosis, Ventricular hypertrophyView all (50 more) |
|
530
|
|
|
Peripheral myelin protein 2 |
CMT1G, FABP8, M-FABP, MP2, P2 |
|
