|
531
|
|
|
Peripheral myelin protein 22 |
CIDP, CMT1A, CMT1E, DSS, GAS-3, GAS3, HMSNIA, HNPP, Sp110 |
Charcot-marie-tooth disease, Dejerine-sottas disease, Demyelinating diseases, Developmental disability, Distal spinal muscular atrophy, Myoclonic epilepsy, Hypertrophic neuropathy, Hereditary, neuropathy with liability to pressure palsies, Non-neoplastic peripheral nervous system disease, Paresthesia, Peripheral nervous system disease, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Seasonal allergic rhinitis |
|
532
|
|
|
PMS1 homolog 1, mismatch repair system component |
HNPCC3, MLH2, PMSL1, hPMS1 |
|
|
533
|
|
|
PMS1 homolog 2, mismatch repair system component pseudogene 1 |
PMS2L1, PMS2L13, PMS2L6, PMS2L7, PMS2L8, PMS3, PMS8, PMSR1, PMSR2 |
|
|
534
|
|
|
Pelota mRNA surveillance and ribosome rescue factor |
CGI-17, PRO1770 |
|
|
535
|
|
|
Peptidylprolyl isomerase like 3 |
CYPJ |
|
|
536
|
|
|
PMS1 homolog 2, mismatch repair system component |
HNPCC4, LYNCH4, MLH4, MMRCS4, PMS-2, PMS2CL, PMSL2 |
Breast cancer, Cafe-au-lait spots, Cardiomyopathy, Lynch syndrome, Hereditary breast cancer, Pancreatic cancer, Constitutional mismatch repair deficiency, Muir-torre syndrome, Ocular sarcoidosis, Ovarian cancer, Prostate cancer, Rhabdomyosarcoma, Severe acute respiratory syndrome, Turcot syndrome |
|
537
|
|
|
Paired related homeobox 1 |
AGOTC, PHOX1, PMX1, PRX-1, PRX1 |
Agnathia-otocephaly, Alzheimer disease, Aortic stenosis, Aortic valve disease, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Craniosynostosis, Dementia, Demyelinating diseases, Dysgnathia complex, Otosclerosis, Prostatic neoplasm, Retrognathia, Venous thromboembolismView all (2 more) |
|
538
|
|
|
Poly(rC) binding protein 3 |
ALPHA-CP3, PCBP3-OT1, PCBP3OT |
|
|
539
|
|
|
Pancreatic lipase |
PL, PNLIPD, PTL |
|
|
540
|
|
|
Pancreatic lipase related protein 1 |
PLRP1 |
|
