|
501
|
|
|
Phospholipase C beta 3 |
SMDCD |
|
|
502
|
|
|
Phospholipase C beta 4 |
ARCND2, ARCND2A, ARCND2B, PI-PLC |
Auriculocondylar syndrome, Bipolar disorder, Developmental delay, Dysmorphic features, Glossoptosis, Macrocephaly, Melanoma, Microglossia, Microstomia, Microtia, Multiple congenital anomalies, Ocular melanosis, Periauricular skin pits, Posteriorly rotated ear, Ptosis, Schizoaffective disorder, Schizophrenia, Sleep apnea, Uveal melanoma, Vein of galen aneurysmView all (5 more) |
|
503
|
|
|
Phospholipase C delta 1 |
NDNC3, PLC-III |
|
|
504
|
|
|
Phospholipase C like 1 (inactive) |
PLCE, PLCL, PLDL1, PPP1R127, PRIP |
|
|
505
|
|
|
Phospholipase C gamma 1 |
IDAA, NCKAP3, PLC-II, PLC1, PLC148, PLCgamma1 |
Atrial fibrillation, Bipolar disorder, Coronary artery disease, Coronary heart disease, Diabetes, Diabetes mellitus, Granulomatous slack skin, Heart failure, Hemangiosarcoma, Lymphoma, Malignant neoplasm, Mental depression, Sezary syndrome, Stroke, T-cell lymphoma/leukemia |
|
506
|
|
|
Phospholipase C gamma 2 |
APLAID, FCAS3, PLC-IV, PLC-gamma-2 |
Allergic rhinitis, Alzheimer disease, Antibody deficiency and immune dysregulation, Autoinflammation, antibody deficiency, and immune dysregulation, Autoinflammatory disease, Bronchiolitis, Cold autoinflammatory syndrome, Cold urticaria, Coronary artery disease, Cryopyrin-associated periodic syndromes, Hashimoto disease, Inflammatory bowel disease, Lymphocytic leukemia, Leukemia, Muckle-wells syndrome, Neurological, cutaneous and articular syndrome, Senile dementia, Ulcerative colitis, Urticaria, VitiligoView all (5 more) |
|
507
|
|
|
Phospholipase D1 |
CVDD, CVDP1 |
Cerebral infraction, Developmental cardiac valvular defect, Cerebral thrombosis, Hydronephrosis, Hydrops fetalis, Mitral valve prolapse, Mitral valve stenosis, Patent foramen ovale, Tricuspid atresia, Tricuspid valve insufficiency, Tricuspid valve prolapse |
|
508
|
|
|
Phospholipase D2 |
PLD1C |
|
|
509
|
|
|
Plectin |
EBS1, EBS5A, EBS5B, EBS5C, EBS5D, EBSMD, EBSND, EBSO, EBSOG, EBSPA, HD1, LGMD2Q, LGMDR17, PCN, PLEC1, PLEC1b, PLTN |
Alopecia, Anemia, Anonychia, Aphasia, Aplasia cutis congenita, Arthrogryposis multiplex congenita, Bronchiolitis, Congenital alveolar dysplasia, Bundle branch block, Congenital pyloric atresia, Dental enamel hypoplasia, Developmental delay, Dwarfism, Dysphagia, Dysphasia, Ectropion, Epidermolysa bullosa simplex and limb girdle muscular dystrophy, Epidermolysis bullosa, Epidermolysis bullosa simplex, Epidermolysis bullosa simplex with muscular dystrophy, Epidermolysis bullosa simplex with nail dystrophy, Epidermolysis bullosa simplex with pyloric atresia, Epidermolysis bullosa simplex without extracutaneous involvement, Esophageal atresia, Glomerulonephritis, Glomerulosclerosis, Hydronephrosis, Junctional split, Keratitis, Lambert-eaton myasthenic syndrome, Limb-girdle muscular dystrophy, Microtia, Motor delay, Muscular dystrophy, Myasthenia gravis, Myasthenic syndrome, Myopathy, Nail diseases, Nail dysplasia, Nail dystrophy, Oculomotor nerve palsy, Onychogryposis, Osteoarthritis of hip, Palmoplantar keratosis, Ptosis, Pulmonary fibrosis, Punctate keratitis, Renal dysplasia, Skin erosion, Ureterocele, Urogenital abnormalitiesView all (36 more) |
|
510
|
|
|
Plasminogen |
HAE4 |
Angioedema, Bronchitis, Cerebellar hypoplasia, Conjunctivitis, Coronary artery disease, Dandy-walker syndrome, Developmental delay, Duodenal ulcer, Excessive tearing, Congenital gallbladder anomaly, Gastrointestinal inflammation, Gingivitis, Hydrocephalus, Hypertension, Hypoplasminogenemia, Keratoconjunctivitis, Kidney failure, Leukocyte disorders, Ligneous conjunctivitis, Macrocephaly, Mental depression, Nephritis, Nephrolithiasis, Otitis media, Periodontitis, Plasminogen deficiency, Acute kidney insufficiency, Schizophrenia, Stomatitis, Temporal arteritis, Thrombosis, Uterine cervicitis, VaginitisView all (18 more) |
