Medical Conditions — P
39 conditions found
PAGOD syndromeQ87.8Palmoplantar keratoderma, Nagashima typeQ82.8Papillary intralymphatic angioendotheliomaD18.1Partial atrioventricular septal defect without ventricular hypoplasiaQ21.2Partial deletion of chromosome 16 syndromeQ93.5Partial deletion of the long arm of chromosome 14 syndromeQ93.5Partial deletion of the short arm of chromosome 2 syndromeQ93.4Partial duplication of chromosome 17 syndromeQ99.8Partial duplication of the long arm of chromosome 10 syndromeQ99.8Pediatric arterial ischemic strokeI63.9Pediatric hepatocellular carcinomaC22.0Peripheral fast-flow vascular malformationQ27.3Peroxisomal acyl-CoA oxidase deficiencyE71.3Phakomatosis cesioflammeaQ82.5Phosphoserine aminotransferase deficiency, infantile/juvenile formE72.09PIBIDS syndromeQ84.2Pituitary apoplexyD35.2Pituitary stalk interruption syndromeE23.0Polyarticular juvenile idiopathic arthritisM08.0Postaxial polydactyly type BQ69.1Postaxial polydactyly-dental and vertebral anomalies syndromeQ69.2PPARG-related familial partial lipodystrophyE88.1Precursor B-cell acute lymphoblastic leukemiaC91.0Primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndromeK75.4Primary bone and joint tuberculosisA18.0Primary ciliary dyskinesia-retinitis pigmentosa syndromeQ87.89Primary intestinal lymphangiectasiaK90.4Primary lymphedema without systemic or visceral involvementI89.0Progeria-short stature-pigmented nevi syndromeQ87.1Progeroid syndrome, Petty typeQ87.1Progressive myoclonic epilepsyG40.3Proteus-like syndromeQ87.3Pseudohypoaldosteronism type 2AE26.89Pterin-4 alpha-carbinolamine dehydratase deficiencyE70.8Pulmonary arterial hypertension associated with connective tissue diseaseI27.0Pulmonary arterial hypertension associated with schistosomiasisI27.2Pulmonary blastomaC34.8Punctate acrokeratoderma freckle-like pigmentationL87.8Pure hair and nail ectodermal dysplasiaQ84.2