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- PABPN1: poly(A) binding protein, nuclear 1
- PAH: phenylalanine hydroxylase
- PALB2: partner and localizer of BRCA2
- PANK2: pantothenate kinase 2 (Hallervorden-Spatz syndrome)
- PARK2: Parkinson disease (autosomal recessive, juvenile) 2, parkin
- PARK7: Parkinson disease (autosomal recessive, early onset) 7
- PAX2: paired box 2
- PAX3: paired box 3
- PAX8: paired box 8
- PC: pyruvate carboxylase
- PCBD1: pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha
- PCCA: propionyl Coenzyme A carboxylase, alpha polypeptide
- PCCB: propionyl Coenzyme A carboxylase, beta polypeptide
- PCDH15: protocadherin 15
- PCSK9: proprotein convertase subtilisin/kexin type 9
- PDCD10: programmed cell death 10
- PHOX2B: paired-like homeobox 2b
- PIGA: phosphatidylinositol glycan anchor biosynthesis, class A (paroxysmal nocturnal hemoglobinuria)
- PINK1: PTEN induced putative kinase 1
- PKD1: polycystic kidney disease 1 (autosomal dominant)
- PKD2: polycystic kidney disease 2 (autosomal dominant)
- PKHD1: polycystic kidney and hepatic disease 1 (autosomal recessive)
- PLA2G6: phospholipase A2, group VI (cytosolic, calcium-independent)
- PLEC1: plectin 1, intermediate filament binding protein 500kDa
- PLOD1: procollagen-lysine 1, 2-oxoglutarate 5-dioxygenase 1
- PLP1: proteolipid protein 1 (Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated)
- PMP22: peripheral myelin protein 22
- PMS2: PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
- PNKD: paroxysmal nonkinesigenic dyskinesia
- PNPLA2: patatin-like phospholipase domain containing 2
- PNPO: pyridoxamine 5'-phosphate oxidase
- POU3F4: POU class 3 homeobox 4
- PPOX: protoporphyrinogen oxidase
- PPP1R12A: protein phosphatase 1, regulatory (inhibitor) subunit 12A
- PRKAG2: protein kinase, AMP-activated, gamma 2 non-catalytic subunit
- PRNP: prion protein (p27-30) (Creutzfeldt-Jakob disease, Gerstmann-Strausler-Scheinker syndrome, fatal familial insomnia)
- PRODH: proline dehydrogenase (oxidase) 1
- PROK2: prokineticin 2
- PROKR2: prokineticin receptor 2
- PRPH: peripherin
- PRPH2: peripherin 2 (retinal degeneration, slow)
- PRX: periaxin
- PSAP: prosaposin (variant Gaucher disease and variant metachromatic leukodystrophy)
- PSEN1: presenilin 1
- PSEN2: presenilin 2 (Alzheimer disease 4)
- PTCH1: patched homolog 1 (Drosophila)
- PTEN: phosphatase and tensin homolog (mutated in multiple advanced cancers 1)
- PTPN11: protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1)
- PTS: 6-pyruvoyltetrahydropterin synthase
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Published: January 23, 2009
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