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Pachydermoperiostosis |
Pachygyria |
Pachyonychia Congenita |
Pachyonychia congenita Jackson Lawler type |
Pacman syndrome |
Paes Whelan Modi syndrome |
Paget disease extramammary |
Paget disease juvenile type |
Paget's Disease |
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 Mosaic Syndrome |
Pallister W Syndrome |
Palmer Pagon syndrome |
Palmitoyl-protein thioesterase deficiency |
Palmoplantar Keratoderma |
Palmoplantar porokeratosis of Mantoux |
Palsy cerebral |
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 Tumor |
Pancreatic islet cell tumors |
Pancreatic lipomatosis duodenal stenosis |
Pancreatitis, hereditary |
Pancreatoblastoma |
PANDAS |
Panhypopituitarism |
Panic Anxiety Syndrome |
Panic disorder |
Panmyelophthisis aplastic anemia |
Panniculitis |
Panniculitis, Idiopathic Nodular |
Panophobia |
Panostotic fibrous dysplasia |
Panthophobia |
Papilledema |
Papillion-Lefevre syndrome |
Papillitis |
Papilloma of choroid plexus |
Papillon Lefevre Syndrome |
Papular mucinosis |
Papular urticaria |
Paracoccidioidomycosis |
Paraganglioma |
Parainfluenza virus type 3 antenatal infection |
Paramyotonia Congenita |
Paramyotonia congenita of Von Eulenburg |
Paraneoplastic cerebellar degeneration |
Paraomphalocele |
Paraparesis amyotrophy of hands and feet |
Paraphilia |
Paraplegia |
Paraplegia, Hereditary Spastic |
Paraplegia-brachydactyly-cone shaped epiphysis |
Paraplegia-mental retardation-hyperkeratosis |
Parapsoriasis |
Parasitophobia |
Parastremmatic dwarfism |
Parathyroid cancer |
Parathyroid neoplasm |
Paratyphoid fever |
PARC syndrome |
Parenchymatous cortical degeneration of cerebellum |
Paris-Trousseau thrombopenia |
Parkes-Weber syndrome |
Parkinson dementia Steele type |
Parkinsonism |
Parkinsonism early onset mental retardation |
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 |
Parvovirus antenatal infection |
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 |
Patent ductus arteriosus familial |
Pathophobia |
Patterson Lowry syndrome |
Patterson pseudoleprechaunism syndrome |
Patterson Stevenson syndrome |
Patulous Eustachian Tube |
Pauciarticular chronic arthritis |
Pavone Fiumara Rizzo syndrome |
Peanut Hypersensitivity |
Pearson's marrow/pancreas syndrome |
Pediatric Cardiomyopathy |
Pediatric T-cell leukemia |
Pediculosis |
Peeling Skin Syndrome |
PEHO syndrome |
Pelizaeus Merzbacher Brain Sclerosis |
Pelizaeus-Merzbacher disease |
Pelizaeus-Merzbacher disease, recessive, acute infantile |
Pelizaeus-Merzbacher leukodystrophy |
Pellagra like syndrome |
Pellagrophobia |
Pelvic dysplasia arthrogryposis of lower limbs |
Pelvic inflammatory disease |
Pelvic lipomatosis |
Pelvic shoulder dysplasia |
Pemphigus |
Pemphigus and fogo selvagem |
Pemphigus foliaceus |
Pemphigus vulgaris |
Pemphigus vulgaris, familial |
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 |
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, Congenital Bilateral |
Peritonitis |
Periventricular laminar heterotopia |
Periventricular leukomalacia |
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 planus |
Peters anomaly |
Peters anomaly with cataract |
Peters congenital glaucoma |
Petit Fryns syndrome |
Petty Laxova Wiedemann syndrome |
Peutz Jeghers Syndrome |
Peyronie Disease |
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 Syndrome Type I |
Pfeiffer Tietze Welte syndrome |
Pfeiffer type acrocephalosyndactyly |
PHACE association |
Phacomatosis fourth |
Phacomatosis pigmentokeratotica |
Phacomatosis pigmentovascularis |
Phalacrophobia |
Pharmacophobia |
Phelan-McDermid Syndrome |
Phenobarbital antenatal infection |
Phenobarbital embryopathy |
Phenol sulfotransferase deficiency |
Phenothiazine antenatal infection |
Phenylalanine hydroxylase deficiency |
Phenylalaninemia |
Phenylketonuria |
Phenylketonuria type II |
Phenylketonuric embryopathy |
Pheochromocytoma |
Pheochromocytoma as part of NF |
Philadelphia-negative chronic myeloid leukemia |
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 |
Phosphoglucomutase deficiency type 1 |
Phosphoglucomutase deficiency type 2 |
Phosphoglucomutase deficiency type 3 |
Phosphoglucomutase deficiency type 4 |
Phosphoglycerate kinase 1 deficiency |
Phosphoglycerate Kinase Deficiency |
Phosphomannoisomerase deficiency |
Phosphoribosylpyrophosphate synthetase deficiency |
Photoaugliaphobia |
Photosensitive epilepsy |
Phthiriophobia |
Physical urticaria |
Phytanic acid oxidase deficiency |
PIBIDS syndrome |
Pica |
Picardi-Lassueur-Little syndrome |
Pick disease of the brain |
Pickardt syndrome |
Pick's Disease |
Pie Torcido |
Piebald trait neurologic defects |
Piebaldism |
Piepkorn Karp Hickoc syndrome |
Pierre Marie cerbellar ataxia |
Pierre Robin Sequence |
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 |
Pigmentary retinopathy |
Pigment-dispersion syndrome |
Pigmented villonodular synovitis |
Pignata guarino syndrome |
Pili canulati |
Pili multigemini |
Pili torti |
Pili torti developmental delay neurological abnormalities |
Pili torti nerve deafness |
Pili torti onychodysplasia |
Pillay syndrome |
Pilo dento ungular dysplasia microcephaly |
Pilonidal cyst |
Pilotto syndrome |
Pineal Cysts, Symptomatic |
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 |
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 |
Pleuropulmonary Blastoma |
Plexosarcoma |
Plum syndrome |
Plummer-Vinson syndrome |
Pneumoconiosis |
Pneumocystis jiroveci pneumonia |
Pneumocystosis |
Pneumonia, Eosinophilic |
Pneumonia, Interstitial |
Pneumothorax |
Podder-Tolmie syndrome |
POEMS Syndrome |
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 |
Poland Syndrome |
Poliomyelitis (Polio) |
Poliosophobia |
Polyarteritis |
Polyarteritis Nodosa |
Polyarthritis |
Polyarthritis, systemic |
Polychondritis |
Polycystic kidney disease |
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 Diseases |
Polycystic Liver Disease |
Polycystic ovarian disease, familial |
Polycystic ovaries urethral sphincter dysfunction |
Polycystic Ovary Syndrome |
Polycythemia Vera |
Polydactyly |
Polydactyly alopecia seborrheic dermatitis |
Polydactyly cleft lip palate psychomotor retardation |
Polydactyly myopia syndrome |
Polydactyly postaxial |
Polydactyly postaxial dental and vertebral |
Polydactyly postaxial with median cleft of upper lip |
Polydactyly preaxial type 1 |
Polydactyly syndrome middle ray duplication |
Polydactyly visceral anomalies cleft lip palate |
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 |
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 |
Pompe Disease |
Poncet-Spiegler's cylindroma |
Pontoneocerebellar Hypoplasia |
Popliteal pterygium syndrome |
Popliteal pterygium syndrome lethal type |
Porencephaly |
Porencephaly cerebellar hypoplasia malformations |
Porokeratosis of Mibelli |
Porokeratosis plantaris palmaris et disseminata |
Porokeratosis punctata palmaris et plantaris |
Porphyria |
Porphyria Cutanea Tarda |
Porphyria cutanea tarda, familial type |
Porphyria cutanea tarda, sporadic type |
Porphyria, Acute Intermittent |
Porphyria, ALA-D |
Porphyria, Congenital Erythropoietic |
Porphyria, Hereditary Coproporphyria |
Porphyria, Variegate |
Portal hypertension |
Portal hypertension due to infrahepatic block |
Portal thrombosis |
Portal vein thrombosis |
Portuguese type amyloidosis |
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) |
Potophobia |
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 |
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 |
Precocious puberty, gonadotropin-dependent |
Precocious puberty, male limited |
Preeclampsia |
Preeyasombat Viravithya syndrome |
Pregnancy toxemia /hypertension |
Prekallikrein deficiency, congenital |
Premature aging |
Premature aging, Okamoto type |
Premature atherosclerosis photomyoclonic epilepsy |
Premature menopause, familial |
Premature ovarian failure |
Premenstrual dysphoric disorder |
Prenatal infections |
Presbycusis |
Prieto Badia Mulas syndrome |
Prieur Griscelli syndrome |
Primary agammaglobulinemia |
Primary aldosteronism |
Primary alveolar hypoventilation |
Primary amenorrhea |
Primary biliary cirrhosis |
Primary ciliary dyskinesia |
Primary ciliary dyskinesia, 2 |
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 |
Procarcinoma |
Proconvertin deficiency, congenital |
Proctitis |
Progeria |
Progeria short stature pigmented nevi |
Progeria variant syndrome Ruvalcaba type |
Progeria, Hutchinson Gilford |
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 Myoclonus Epilepsy |
Progressive myositis ossificans |
Progressive Osseous Heteroplasia (POH) |
Progressive spinal muscular atrophy |
Progressive Supranuclear Palsy |
Progressive supranuclear palsy atypical |
Progressive systemic sclerosis |
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 R deficiency |
Protein S acquired deficiency |
Protein S deficiency |
Protein-energy malnutrition |
Proteus like syndrome mental retardation eye defect |
Proteus Syndrome |
Prothrombin deficiency |
Protoporphyria |
Protoporphyria, erythropoietic |
Proud Levine Carpenter syndrome |
Proximal myotonic dystrophy |
Proximal myotonic myopathy |
Proximal spinal muscular atrophy |
Proximal tubulopathy diabetes mellitus cerebellar ataxia |
Prune Belly Syndrome |
Prurigo nodularis |
Psellismophobia |
Pseudo Hurler Polydystrophy |
Pseudoachondroplasia |
Pseudoachondroplastic Dysplasia |
Pseudoachondroplastic dysplasia 1 |
Pseudoadrenoleukodystrophy |
Pseudoaminopterin syndrome |
Pseudoarylsulfatase A deficiency |
Pseudocholinesterase Deficiency |
Pseudo-Gaucher disease |
Pseudogout |
Pseudohermaphrodism anorectal anomalies |
Pseudohermaphroditism |
Pseudohermaphroditism female skeletal anomalies |
Pseudohermaphroditism male with gynecomastia |
Pseudohermaphroditism mental retardation |
Pseudohypoaldosteronism |
Pseudohypoaldosteronism type 1 |
Pseudohypoaldosteronism type 2 |
Pseudohypoparathyroidism |
Pseudomarfanism |
Pseudomonas stutzeri infections |
Pseudomongolism |
Pseudomyxoma Peritonei |
Pseudoobstruction idiopathic intestinal |
Pseudopapilledema blepharophimosis hand anomalies |
Pseudo-Pelade of Brocq |
Pseudopolycythaemia |
Pseudoprogeria syndrome |
Pseudo-torch syndrome |
Pseudotumor Cerebri |
Pseudo-Turner syndrome |
Pseudovaginal perineoscrotal hypospadias |
Pseudoxanthoma Elasticum (PXE) |
Pseudoxanthoma elasticum, dominant form |
Pseudoxanthoma elasticum, recessive form |
Pseudo-Zellweger syndrome |
Psittacosis |
Psoriasis |
Psoriatic arthritis |
Psoriatic rheumatism |
Psychogenic polydipsia |
Psychophysiologic Disorders |
Pterigium Colli |
Pteromerhanophobia |
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 |
Pubic lice |
Puerperal fever |
Pulmonar arterioveinous aneurysm |
Pulmonary agenesis |
Pulmonary Alveolar Proteinosis |
Pulmonary alveolar proteinosis, congenital |
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 |
Pulmonary Hypertension, Primary |
Pulmonary Hypertension, Secondary |
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 |
Pulmonic stenosis with Caf?au lait spot |
Punctate acrokeratoderma freckle like pigmentation |
Punctate inner choroidopathy |
Pupaphobia |
Pure Red Cell Aplasia, Acquired |
Puretic syndrome |
Purine nucleoside phosphorylase deficiency |
Purpura, Henoch-Schonlein |
Purpura, Idiopathic Thrombocytopenic |
Purpura, Schoenlein-Henoch |
Purpura, Thrombotic Thrombocytopenic |
Purtilo syndrome |
Pycnodysostosis |
Pyelonephritis |
Pyknoachondrogenesis |
Pyknodysostosis |
Pyle disease |
Pyoderma Gangrenosum |
Pyomyositis |
Pyrexiophobia |
Pyridoxine deficit |
Pyridoxine-Dependent Seizures |
Pyrimidinemia familial |
Pyrophobia |
Pyropoikilocytosis |
Pyrosis |
Pyruvate Carboxylase Deficiency |
Pyruvate decarboxylase deficiency |
Pyruvate Dehydrogenase Deficiency |
Pyruvate Kinase Deficiency |
Pyruvate kinase deficiency, liver type |
Pyruvate kinase deficiency, muscle type |