List of diseases (P)
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A list of diseases in the English Wikipedia.
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Diseases |
Pa
Pac-Pal
- Pachydermoperiostosis
- Pachygyria
- Pachyonychia congenita Jackson Lawler type
- Pacman syndrome
- Paes Whelan Modi syndrome
- Paget disease extramammary
- Paget disease juvenile type
- Paget's disease of bone
- Paget's disease of the breast
- Paget's disease, type 1
- Pagon Bird Detter syndrome
- Pagon Stephan syndrome
- Pai Levkoff syndrome
- Palant cleft palate syndrome
- Palindromic rheumatism
- Pallister-Hall syndrome
- Pallister-Killian syndrome
- Palmer Pagon syndrome
- Palmitoyl-protein thioesterase deficiency
- Palmoplantar Keratoderma
- Palmoplantar porokeratosis of Mantoux
- Palsy cerebral
Pan
- Pancreas agenesis
- Pancreas divisum
- Pancreatic adenoma
- Pancreatic beta cell agenesis with neonatal diabetes mellitus
- Pancreatic cancer
- Pancreatic carcinoma, familial
- Pancreatic diseases
- Pancreatic islet cell neoplasm
- Pancreatic islet cell tumors
- Pancreatic lipomatosis duodenal stenosis
- Pancreatitis, hereditary
- Pancreatoblastoma
- PANDAS
- Panhypopituitarism
- Panic disorder
- Panmyelophthisis aplastic anemia
- Panniculitis
- Panophobia
- Panostotic fibrous dysplasia
- Panthophobia
Pap
- Papilledema
- Papillion-Lefevre syndrome
- Papillitis
- Papilloma of choroid plexus
- Papular mucinosis
- Papular urticaria
Par
Para-Pari
- Paracoccidioidomycosis
- Paraganglioma
- Parainfluenza virus type 3 antenatal infection
- Paramyotonia congenita of Von Eulenburg
- Paramyotonia congenita
- Paraneoplastic cerebellar degeneration
- Paraomphalocele
- Paraparesis amyotrophy of hands and feet
- Paraphilia
- Paraplegia
- Paraplegia-brachydactyly-cone shaped epiphysis
- Paraplegia-mental retardation-hyperkeratosis
- Parapsoriasis
- Parasitophobia
- Parastremmatic dwarfism
- Parathyroid cancer
- Parathyroid neoplasm
- Paratyphoid fever
- PARC syndrome
- Parcopresis
- Parenchymatous cortical degeneration of cerebellum
- Paris-Trousseau thrombopenia
Park-Parv
- Parkes-Weber syndrome
- Parkinson's disease
- Parkinson dementia Steele type
- Parkinsonism early onset mental retardation
- Parkinsonism
- Parkinson's disease
- Paroxysmal cold hemoglobinuria
- Paroxysmal dystonic choreoathetosis
- Paroxysmal nocturnal hemoglobinuria
- Paroxysmal ventricular fibrillation
- Parry-Romberg syndrome
- Pars planitis
- Parsonage Turner syndrome
- Partial agenesis of corpus callosum
- Partial atrioventricular canal
- Partial deletion of Y
- Partial gigantism in context of NF
- Partial lissencephaly
- Partington Anderson syndrome
- Partington Mulley syndrome
- Parturiphobia
- Paruresis
- Parvovirus antenatal infection
Pas-Pat
- Pascuel Castroviejo syndrome
- Pashayan syndrome
- Pat1
- Pat11
- Pat111
- Pat12
- Pat121
- Pat13
- Pat131
- Pat132
- Pat14
- Pat141
- Pat142
- Patau syndrome
- Patel Bixler syndrome
- Patella aplasia, coxa vara, tarsal synostosis
- Patella hypoplasia mental retardation
- Patent ductus arteriosus familial
- Patent ductus arteriosus
- Patterson Lowry syndrome
- Patterson pseudoleprechaunism syndrome
- Patterson Stevenson syndrome
Pau-Pav
Pe
Pea-Pem
- Peanut hypersensitivity
- Pearson's marrow/pancreas syndrome
- Pediatric T-cell leukemia
- Pediculosis
- Peeling skin syndrome ichthyosis
- PEHO syndrome
- Pelizaeus-Merzbacher brain sclerosis
- Pelizaeus-Merzbacher disease, recessive, acute infantile
- Pelizaeus-Merzbacher disease
- Pelizaeus-Merzbacher leukodystrophy
- Pellagra like syndrome
- Pellagrophobia
- Pelvic dysplasia arthrogryposis of lower limbs
- Pelvic inflammatory disease
- Pelvic lipomatosis
- Pelvic shoulder dysplasia
- Pemphigus and fogo selvagem
- Pemphigus foliaceus
- Pemphigus vulgaris, familial
- Pemphigus vulgaris
- Pemphigus
Pen-Pep
- Pena Shokeir syndrome
- Pendred syndrome
- Penis agenesia
- Penoscrotal transposition
- Penta X syndrome
- Pentalogy of Cantrell
- Pentosuria
- Penttinen-Aula syndrome
- PEPCK 1 deficiency
- PEPCK 2 deficiency
- PEPCK deficiency, mitochondrial
- Peptidic growth factors deficiency
Per
Peri
- Periarteritis nodosa
- Pericardial constriction growth failure
- Pericardial defect diaphragmatic hernia
- Pericardium absent mental retardation short stature
- Pericardium congenital anomaly
- Perilymphatic fistula
- Perimyositis
- Perinatal infections
- Periodic disease
- Periodic fever, aphthous stomatitis, pharyngitis and adenitis
- Periodontal disease / Periodontitis
- Peripartum cardiomyopathy
- Peripheral blood vessel disorder
- Peripheral nervous disorder
- Peripheral neuroectodermal tumor
- Peripheral neuropathy
- Peripheral T-cell lymphoma
- Peripheral type neurofibromatosis
- Perisylvian syndrome
- Peritonitis
- Periventricular laminar heterotopia
- Periventricular leukomalacia
Pern-Pert
- Pernicious anemia
- Perniola Krajewska Carnevale syndrome
- Perniosis
- Peroxisomal Bifunctional Enzyme Deficiency
- Peroxisomal defects
- Persistent Mullerian duct syndrome (PMDS)
- Persistent parvovirus infection
- Persistent sexual arousal syndrome
- Persistent truncus arteriosus
- Pertussis
Pes-Pey
- Pes planus
- Peters anomaly with cataract
- Peters anomaly
- Peters congenital glaucoma
- Petit Fryns syndrome
- Petty Laxova Wiedemann syndrome
- Peutz-Jeghers syndrome
- Peyronie disease
Pf
- Pfeiffer cardiocranial syndrome
- Pfeiffer Hirschfelder Rott syndrome
- Pfeiffer Kapferer syndrome
- Pfeiffer Mayer syndrome
- Pfeiffer Palm Teller syndrome
- Pfeiffer Rockelein syndrome
- Pfeiffer Singer Zschiesche syndrome
- Pfeiffer syndrome
- Pfeiffer Tietze Welte syndrome
- Pfeiffer type acrocephalosyndactyly
Ph
Pha-Phi
- PHACE association
- Phacomatosis fourth
- Phacomatosis pigmentokeratotica
- Phacomatosis pigmentovascularis
- Phalacrophobia
- Pharmacophobia
- Phenobarbital antenatal infection
- Phenobarbital embryopathy
- Phenol sulfotransferase deficiency
- Phenothiazine antenatal infection
- Phenylalanine hydroxylase deficiency
- Phenylalaninemia
- Phenylketonuria type II
- Phenylketonuria
- Phenylketonuric embryopathy
- Pheochromocytoma as part of NF
- Pheochromocytoma
- Philadelphia-negative chronic myeloid leukemia
Pho-Pht
- Phocomelia contractures absent thumb
- Phocomelia ectrodactyly deafness sinus arrhythmia
- Phocomelia Schinzel type
- Phocomelia syndrome
- Phocomelia thrombocytopenia encephalocele
- Phosphate diabetes
- Phosphoenolpyruvate carboxykinase 1 deficiency
- Phosphoenolpyruvate carboxykinase 2 deficiency
- Phosphoenolpyruvate carboxykinase deficiency
- Phosphoglucomutase deficiency type 1
- Phosphoglucomutase deficiency type 2
- Phosphoglucomutase deficiency type 3
- Phosphoglucomutase deficiency type 4
- Phosphoglucomutase deficiency
- Phosphoglycerate kinase 1 deficiency
- Phosphoglycerate kinase deficiency
- Phosphomannoisomerase deficiency
- Phosphoribosylpyrophosphate synthetase deficiency
- Photoaugliaphobia
- Photosensitive epilepsy
- Phthiriophobia
Phy
Pi
Pib-Pig
- PIBIDS syndrome
- Pica
- Picardi-Lassueur-Little syndrome
- Pick disease of the brain
- Pickardt syndrome
- Pie Torcido
- Piebald trait neurologic defects
- Piebaldism
- Piepkorn Karp Hickoc syndrome
- Pierre Marie cerbellar ataxia
- Pierre Robin sequence congenital heart defect talipes
- Pierre Robin sequence faciodigital anomaly
- Pierre Robin syndrome fetal chondrodysplasia
- Pierre Robin syndrome hyperphalangy clinodactyly
- Pierre Robin syndrome skeletal dysplasia polydactyly
- Pierre Robin's sequence
- Pigmentary retinopathy
- Pigment-dispersion syndrome
- Pigmented villonodular synovitis
- Pignata guarino syndrome
Pil-Piu
- Pili canulati
- Pili multigemini
- Pili torti developmental delay neurological abnormalities
- Pili torti nerve deafness
- Pili torti onychodysplasia
- Pili torti
- Pillay syndrome
- Pilo dento ungular dysplasia microcephaly
- Pilonidal cyst
- Pilotto syndrome
- Pinealoma
- Pinheiro Freire Maia Miranda syndrome
- Pinsky Di George Harley syndrome
- Pinta
- Pipecolic acidemia
- PIRA
- Pitt Hopkins syndrome
- Pitt-Rogers-Danks syndrome
- Pituitary dwarfism 1
- Pityriasis lichenoides chronica
- Pityriasis lichenoides et varioliformis acuta
- Pityriasis rubra pilaris
- Piussan Lenaerts Mathieu syndrome
Pl-Pn
- Placenta disorder
- Placenta neoplasm
- Placental abruption
- Plagiocephaly X linked mental retardation
- Plague (bubonic, septicemic, pneumonic and pharyngeal)
- Plasmacytoma anaplastic
- Plasmalogenes synthesis deficiency isolated
- Plasminogen activitor inhibitor type 1 deficiency, congenital
- Plasminogen deficiency, congenital
- Platelet disorder
- Platyspondylic lethal chondrodysplasia
- Platyspondyly amelogenesis imperfecta
- Pleural effusion
- Pleuritis
- Pleuritis
- Plexosarcoma
- Plum syndrome
- Plummer-Vinson syndrome
- Pneumoconiosis
- Pneumocystis jiroveci pneumonia
- Pneumocystosis
- Pneumonia, eosinophilic
- Pneumonoultramicroscopicsilicovolcanoconiosis
- Pneumothorax
Po
Pod-Poi
- Podder-Tolmie syndrome
- POEMS syndrome
- Poedimus kyleopecia mental retardation
- Poikiloderma congenital with bullae Weary type
- Poikiloderma hereditary acrokeratotic Weary type
- Poikiloderma of Kindler
- Poikiloderma of Rothmund-Thomson
- Poikilodermatomyositis mental retardation
- Poikilodermia alopecia retrognathism cleft palate
- Pointer syndrome
Pol
Pola-Poli
Poly
Polya-Polyc
- Polyarteritis nodosa
- Polyarteritis
- Polyarthritis, systemic
- Polyarthritis
- Polychondritis
- Polycystic kidney disease, adult type
- Polycystic kidney disease, infantile type
- Polycystic kidney disease, infantile, type I
- Polycystic kidney disease, recessive type
- Polycystic kidney disease, type 1
- Polycystic kidney disease, type 2
- Polycystic kidney disease, type 3
- Polycystic kidney disease
- Polycystic ovarian disease, familial
- Polycystic ovarian syndrome
- Polycystic ovaries urethral sphincter dysfunction
- Polycythemia vera
Polyd-Polyo
- Polydactyly alopecia seborrheic dermatitis
- Polydactyly cleft lip palate psychomotor retardation
- Polydactyly myopia syndrome
- Polydactyly postaxial dental and vertebral
- Polydactyly postaxial with median cleft of upper lip
- Polydactyly postaxial
- Polydactyly preaxial type 1
- Polydactyly syndrome middle ray duplication
- Polydactyly visceral anomalies cleft lip palate
- Polydactyly
- Polyglucosan body disease, adult
- Polymicrogyria turricephaly hypogenitalism
- Polymorphic catecholergic ventricular tachycardia
- Polymorphic macular degeneration
- Polymorphous low-grade adenocarcinoma
- Polymyalgia rheumatica
- Polymyositis
- Polyneuritis
- Polyneuropathy hand defect
- Polyneuropathy mental retardation acromicria prema
- Polyomavirus Infections
- Polyostotic fibrous dysplasia
Polyp-Polys
- Polyposis, hamartomatous intestinal
- Polyposis skin pigmentation alopecia fingernail changes
- Polysyndactyly cardiac malformation
- Polysyndactyly microcephaly ptosis
- Polysyndactyly orofacial anomalies
- Polysyndactyly overgrowth syndrome
- Polysyndactyly trigonocephaly agenesis of corpus callosum
- Polysyndactyly type 4
- Polysyndactyly type Haas
Pom-Por
- Pompe's disease
- Poncet-Spiegler's cylindroma
- Pontoneocerebellar Hypoplasia
- Popliteal pterygium syndrome lethal type
- Popliteal pterygium syndrome
- Porencephaly cerebellar hypoplasia malformations
- Porencephaly
- Porokeratosis of Mibelli
- Porokeratosis plantaris palmaris et disseminata
- Porokeratosis punctata palmaris et plantaris
- Porphyria
- Porphyria cutanea tarda, familial type
- Porphyria cutanea tarda, sporadic type
- Porphyria cutanea tarda
- Porphyria, acute intermittent
- Porphyria, Ala-D
- Porphyria, congenital erythropoietic
- Porphyria, hereditary coproporphyria
- Portal hypertension due to infrahepatic block
- Portal hypertension
- Portal thrombosis
- Portal vein thrombosis
- Portuguese type amyloidosis
Pos-Pox
- Positive rheumatoid factor polyarthritis
- Post Polio syndrome
- Post Traumatic Stress disorder (PTSD)
- Postaxial polydactyly mental retardation
- Posterior tibial tendon rupture
- Posterior urethral valves
- Posterior uveitis
- Posterior valve urethra
- Post-infectious myocarditis
- Post-traumatic epilepsy
- Postural hypotension
- Potassium aggravated myotonia
- Potassium deficiency (hypokalemia)
- Potter disease type 1
- Potter disease, type 3
- Potter sequence cleft cardiopathy
- Potter syndrome dominant type
- Powell Buist Stenzel syndrome
- Powell Chandra Saal syndrome
- Powell Venencie Gordon syndrome
- Poxviridae disease
Pr
Pra-Pre
- Prader-Willi syndrome
- Prata Liberal Goncalves syndrome
- Preaxial deficiency postaxial polydactyly hypospadia
- Preaxial polydactyly colobomata mental retardation
- Precocious epileptic encephalopathy
- Precocious myoclonic encephalopathy
- Precocious puberty, gonadotropin-dependent
- Precocious puberty, male limited
- Precocious puberty
- Preeclampsia
- Preeyasombat Viravithya syndrome
- Pregnancy toxemia /hypertension
- Prekallikrein deficiency, congenital
- Premature aging, Okamoto type
- Premature aging
- Premature atherosclerosis photomyoclonic epilepsy
- Premature menopause, familial
- Premature ovarian failure
- Premenstrual dysphoric disorder
- Prenatal infections
- Presbycusis
Pri
- Prieto Badia Mulas syndrome
- Prieur Griscelli syndrome
- Primary agammaglobulinemia
- Primary aldosteronism
- Primary alveolar hypoventilation
- Primary amenorrhea
- Primary biliary cirrhosis
- Primary ciliary dyskinesia, 2
- Primary ciliary dyskinesia
- Primary craniosynostosis
- Primary cutaneous amyloidosis
- Primary granulocytic sarcoma
- Primary hyperoxaluria
- Primary hyperparathyroidism
- Primary lateral sclerosis
- Primary malignant lymphoma
- Primary orthostatic tremor
- Primary progressive aphasia
- Primary pulmonary hypertension
- Primary sclerosing cholangitis
- Primary tubular proximal acidosis
- Primerose syndrome
- Primordial microcephalic dwarfism Crachami type
- Prinzmetal's variant angina
Pro
Proc
Prog
- Progeria short stature pigmented nevi
- Progeria variant syndrome Ruvalcaba type
- Progeria
- Progeroid syndrome De Barsy type
- Progeroid syndrome Petty type
- Progeroid syndrome, Penttinen type
- Prognathism dominant
- Progressive acromelanosis
- Progressive black carbon hyperpigmentation of infancy
- Progressive diaphyseal dysplasia
- Progressive external ophthalmoplegia
- Progressive hearing loss stapes fixation
- Progressive kinking of the hair, acquired
- Progressive multifocal leukoencephalopathy
- Progressive myositis ossificans
- Progressive osseous heteroplasia
- Progressive spinal muscular atrophy
- Progressive supranuclear palsy atypical
- Progressive supranuclear palsy
- Progressive systemic sclerosis
Prol-Prou
- Prolactinoma, familial
- Prolerating trichilemmal cyst
- Prolidase deficiency
- Prolymphocytic leukemia
- Properdin deficiency
- Prosencephaly cerebellar dysgenesis
- Prostaglandin antenatal infection
- Prostate cancer, familial
- Prostatic malacoplakia associated with prostatic abscess
- Prostatitis
- Protein C deficiency
- Protein-energy malnutrition
- Protein R deficiency
- Protein S acquired deficiency
- Protein S deficiency
- Proteus like syndrome mental retardation eye defect
- Proteus syndrome
- Prothrombin deficiency
- Protoporphyria, erythropoietic
- Protoporphyria
- Proud Levine Carpenter syndrome
Prox
- Proximal myotonic dystrophy
- Proximal myotonic myopathy
- Proximal spinal muscular atrophy
- Proximal tubulopathy diabetes mellitus cerebellar ataxia
Pru
Ps
Pse
Psel
Pseu
Pseud
Pseudo
Pseudoa-Pseudom
- Pseudoachondroplasia
- Pseudoachondroplastic dysplasia 1
- Pseudoachondroplastic dysplasia
- Pseudoadrenoleukodystrophy
- Pseudoaminopterin syndrome
- Pseudoarylsulfatase A deficiency
- Pseudocholinesterase deficiency
- Pseudo-Gaucher disease
- Pseudogout
- Pseudohermaphrodism anorectal anomalies
- Pseudohermaphroditism female skeletal anomalies
- Pseudohermaphroditism male with gynecomastia
- Pseudohermaphroditism mental retardation
- Pseudohermaphroditism
- Pseudohypoaldosteronism type 1
- Pseudohypoaldosteronism type 2
- Pseudohypoaldosteronism
- Pseudohypoparathyroidism
- Pseudomarfanism
- Pseudomonas stutzeri infections
- Pseudomongolism
- Pseudomyxoma peritonei
Pseudoo-Pseudo-Z
- Pseudoobstruction idiopathic intestinal
- Pseudopapilledema
- Pseudopapilledema blepharophimosis hand anomalies
- Pseudo-Pelade of Brocq
- Pseudopolycythaemia
- Pseudoprogeria syndrome
- Pseudo-torch syndrome
- Pseudotumor cerebri
- Pseudo-Turner syndrome
- Pseudovaginal perineoscrotal hypospadias
- Pseudoxanthoma elasticum, dominant form
- Pseudoxanthoma elasticum, recessive form
- Pseudoxanthoma elasticum
- Pseudo-Zellweger syndrome
Psi-Psy
- Psittacosis
- Psoriasis
- Psoriatic arthritis
- Psoriatic rheumatism
- Psychogenic polydipsia
- Psychophysiologic Disorders
- Psychosis
Pt
- Pterigium Colli
- Pterygia mental retardation facial dysmorphism
- Pterygium colli mental retardation digital anomalies
- Pterygium of the conjunctiva
- Pterygium syndrome antecubital
- Pterygium syndrome multiple dominant type
- Pterygium syndrome X linked
- Pterygium syndrome, multiple
- Ptosis
- Ptosis coloboma mental retardation
- Ptosis coloboma trigonocephaly
- Ptosis strabismus diastasis
- Ptosis strabismus ectopic pupils
Pu
Pub
Pul
Pulm
Pulmo
Pulmon
- Pulmonar arterioveinous aneurysm
- Pulmonary agenesis
- Pulmonary alveolar proteinosis, congenital
- Pulmonary alveolar proteinosis
- Pulmonary arterio-veinous fistula
- Pulmonary artery agenesis
- Pulmonary artery coming from the aorta
- Pulmonary artery familial dilatation
- Pulmonary atresia with ventricular septal defect
- Pulmonary blastoma
- Pulmonary branches stenosis
- Pulmonary cystic lymphangiectasis
- Pulmonary Disease, Chronic Obstructive
- Pulmonary edema of mountaineers
- Pulmonary fibrosis /granuloma
- Pulmonary Hypertension, Secondary
- Pulmonary hypertension
- Pulmonary hypoplasia familial primary
- Pulmonary sequestration
- Pulmonary supravalvular stenosis
- Pulmonary surfactant protein B, deficiency of
- Pulmonary valve stenosis
- Pulmonary valves agenesis
- Pulmonary veins stenosis
- Pulmonary veno-occlusive disease
- Pulmonary venous return anomaly
- Pulmonaryatresia intact ventricular septum
Pun-Pur
- Punctate acrokeratoderma freckle like pigmentation
- Punctate inner choroidopathy
- Pure red cell aplasia
- Puretic syndrome
- Purine nucleoside phosphorylase deficiency
- Purpura, Schoenlein-Henoch
- Purpura, thrombotic thrombocytopenic
- Purpura
- Purtilo syndrome
Py
- Pyaemia
- Pycnodysostosis
- Pyknoachondrogenesis
- Pyle disease
- Pyelonephritis
- Pyoderma gangrenosum
- Pyomyositis
- Pyridoxine deficit
- Pyrimidinemia familial
- Pyrophobia
- Pyropoikilocytosis
- Pyrosis
- Pyruvate carboxylase deficiency
- Pyruvate decarboxylase deficiency
- Pyruvate dehydrogenase deficiency
- Pyruvate kinase deficiency, liver type
- Pyruvate kinase deficiency, muscle type
- Pyruvate kinase deficiency
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
