Primary Myelofibrosis Pelger Huet Anomaly Peutz Jeghers Syndrome Pheochromocytoma Polycythemia Vera Progeria Pseudopseudohypoparathyroidism Pseudoxanthoma Elasticum Piebaldism Polycystic Kidney, Autosomal Dominant Polycystic Kidney, Autosomal Recessive Porphyria, Erythropoietic Porphyria, Acute Intermittent Pelizaeus Merzbacher Disease Paralysis, Hyperkalemic Periodic Popliteal Pterygium Syndrome Pendred syndrome Pyruvate Kinase Deficiency of Red Cells Peters anomaly Poikiloderma of Kindler Pseudoachondroplasia Periodic fever, familial, autosomal dominant Polymorphic catecholergic ventricular tachycardia Pierson syndrome Papillorenal syndrome Pitt Hopkins syndrome Parkinson Disease 7, Autosomal Recessive Early-Onset Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Purine Nucleoside Phosphorylase Deficiency Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Parkinson Disease 6, Autosomal Recessive Early-Onset Peroxisomal ACYL-COA oxidase deficiency Pulmonary Disease, Chronic Obstructive Prader Willi Syndrome Pyruvate Dehydrogenase Complex Deficiency Disease Porphyria Cutanea Tarda Pallister-Hall Syndrome Peroxisomal bifunctional enzyme deficiency Primary ciliary dyskinesia, 3 Platelet Glycoprotein IV Deficiency Primary ciliary dyskinesia, 2 Pitt-Hopkins-Like Syndrome 1 Persistent Mullerian duct syndrome Parietal Foramina Pierre Robin syndrome with fetal chondrodysplasia Papillon-Lefevre Disease Paraganglioma Phenylketonurias Pityriasis Rubra Pilaris Pilomatrixoma Pick Disease of the Brain Pycnodysostoses Primary hyperoxaluria type 1 Primary hyperoxaluria type 2 Pseudovaginal Perineoscrotal Hypospadias Polyostotic osteolytic dysplasia, hereditary expansile Pleuropulmonary blastoma Paroxysmal Extreme Pain Disorder Polymicrogyria, Bilateral Frontoparietal Pyridoxine-dependent epilepsy Polyglucosan Body Disease, Adult Form Pyogenic arthritis, pyoderma gangrenosum, and acne Poikiloderma with Neutropenia Propping Zerres syndrome Pigmented Nodular Adrenocortical Disease, Primary, 1 Pneumothorax, Primary Spontaneous Perry Syndrome Precursor Cell Lymphoblastic Leukemia-Lymphoma Plasminogen Deficiency, Type I Parkinsonism-Dystonia, Infantile Progressive familial intrahepatic cholestasis 2 Popliteal Pterygium Syndrome, Lethal Type Pontocerebellar Hypoplasia Type 6 Potassium aggravated myotonia Pulmonary Alveolar Microlithiasis Pterygium syndrome, multiple Potocki-Lupski syndrome Primrose syndrome Pallidopyramidal syndrome Phosphoglycerate Kinase 1 Deficiency Posterior column ataxia with retinitis pigmentosa Primary lateral sclerosis juvenile Pretibial epidermolysis bullosa Parkinsonism, early onset with mental retardation Progressive hearing loss stapes fixation Peeling skin syndrome, acral type Pseudohyperkalemia Cardiff Plantar Lipomatosis, Unusual Facies, and Developmental Delay Papilloma, Choroid Plexus Prekallikrein Deficiency Partington X-linked mental retardation syndrome Pyle disease Porphyria, Acute Hepatic Pyropoikilocytosis, Hereditary Pena Shokeir syndrome, type 1 Platelet Disorder, Familial, with Associated Myeloid Malignancy Platyspondylic Lethal Skeletal Dysplasia, Torrance Type PEHO syndrome Patterson Stevenson syndrome Parastremmatic dwarfism Pseudohypoparathyroidism Type 1C Pituitary dwarfism 1 Pontocerebellar Hypoplasia Type 1 Pigmented Paravenous Chorioretinal Atrophy Proliferative Vitreoretinopathies Proprotein Convertase 1 3 Deficiency Pontocerebellar Hypoplasia Type 2A Progressive supranuclear palsy atypical Paragangliomas 4 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency Penttinen-Aula syndrome Paragangliomas 2 Pterygium Syndrome, Multiple, Autosomal Dominant Parietal Foramina With Cleidocranial Dysplasia Phosphoserine Aminotransferase Deficiency Phosphoribosylpyrophosphate Synthetase Superactivity Polymicrogyria With Optic Nerve Hypoplasia Polydactyly, Postaxial, Type A1 Pancreatitides Parkinson Disease Persistent Fetal Circulation Syndrome Pierre Robin Syndrome Polycythemias Prolactinoma Pseudohypoparathyroidism Psoriases Pulmonary Alveolar Proteinosis Pulmonary Fibrosis Purpura, Thrombotic Thrombocytopenic Pyruvate Carboxylase Deficiency Disease Progressive Supranuclear Palsies Proteus Syndrome Polydactyly Polycystic liver disease Pancreatic Carcinoma Parkinsonian Disorders Pentosuria Paroxysmal ventricular fibrillation Pelvi-ureteric junction obstruction Proud Syndrome Pituitary Hormone Deficiency, Combined, 2 Polydactyly preaxial type 1 Peroxisome biogenesis disorders Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Premature Ovarian Failure 3 Pyruvate dehydrogenase phosphatase deficiency Pyruvate Dehydrogenase E1 Alpha Deficiency Properdin deficiency, X-linked Pseudohypoaldosteronism, Type IIb Prolonged Electroretinal Response Suppression Pontocerebellar Hypoplasia Type 3 Pigmentary Disorder, Reticulate, with Systemic Manifestations Premature Ovarian Failure 2b Pelizaeus-Merzbacher-like disease, autosomal recessive, 2 Parkinson Disease 4, Autosomal Dominant Lewy Body Pyruvate Dehydrogenase E3-Binding Protein Deficiency Pyruvate Dehydrogenase E2 Deficiency Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Parietal Foramina 2 Phosphoglycerate Dehydrogenase Deficiency Porokeratosis, disseminated superficial actinic 1 Polydactyly, preaxial 4 Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Premature Ovarian Failure 5 Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy Progressive Familial Heart Block, Type Ib Prickle1-Related Progressive Myoclonic Epilepsy with Ataxia Pontocerebellar Hypoplasia Type 2C Pontocerebellar Hypoplasia Type 2B Pituitary Hormone Deficiency, Combined, 4 Plasminogen Activator Inhibitor-1 Deficiency Pituitary Hormone Deficiency, Combined, 1 Premature Ovarian Failure 7 Prostate cancer, familial Pseudohypoparathyroidism Type 1B Pyruvate Dehydrogenase E1-Beta Deficiency Platelet-Activating Factor Acetylhydrolase Deficiency Paroxysmal nonkinesigenic dyskinesia Pre Eclampsia Port Wine Stain Prune Belly Syndrome Peeling Skin Syndrome Pelviscapular dysplasia Preaxial deficiency, postaxial polydactyly and hypospadias Progeroid Syndrome, Congenital, Petty Type Pseudo-TORCH syndrome Postaxial Polydactyly, Type A Pseudohypoaldosteronism Phosphoenolpyruvate carboxykinase deficiency Polyposis Syndrome, Hereditary Mixed, 1 Proopiomelanocortin Deficiency Pain Insensitivity, Congenital Pain Pancytopenia Pneumonia Proteinuria Puberty, Delayed Peritoneal Fibrosis Pseudohypoaldosteronism, Type IIc Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia Presentey Anomaly Pigmented Nodular Adrenocortical Disease, Primary, 2 Parietal Foramina 1 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Protoporphyria, Erythropoietic, X-Linked Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Polyangiitides, Granulomatosis with Phenylketonuria, Maternal Porencephalies Potocki-Shaffer syndrome PEHO-Like Syndrome Phacomatosis pigmentokeratotica Perisylvian syndrome Porphyria Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Pulmonary Edema Polydactyly, Postaxial Pontocerebellar Hypoplasia Panhypopituitarism X-linked Panbronchiolitis, diffuse Pulmonary alveolar proteinosis, congenital Papilloma Prostatitides Pulmonary Embolism Pulmonary Emphysema Prion Diseases Preterm Premature Rupture of the Membranes Premature Ovarian Failure 2a Pancreatic Agenesis, Congenital Polyglandular Deficiency Syndrome, Persian-Jewish Type Polyposis Syndrome, Hereditary Mixed, 2 Postaxial Polydactyly, Type B Premature Ovarian Failure 6 Pneumothorax Polymicrogyria Puberty, Precocious Prematurity Retinopathies Pyoderma Gangrenosum Paragangliomas 3 Precursor B Cell Lymphoblastic Leukemia Lymphoma Plagiocephalies Partial ADA Deficiency Paresthesia Platelet Storage Pool Deficiency Prolapse Persistent Hyperplastic Primary Vitreous Peripheral Arterial Disease Phyllodes Tumor Penile Induration Polyarteritis Nodosa Periodontitides Periodontitis, Aggressive Pleurisies Polyuria Pruritus Parapareses, Spastic Photophobia Polymyositis Pulmonary Arteriovenous Fistulas Precocious Puberty, Central Partial atrioventricular canal Pituitary Adenoma, Growth Hormone Secreting Partial agenesis of corpus callosum Paralyses Primary Progressive Nonfluent Aphasia Pituitary Adenoma, ACTH-Secreting Parathyroid Glands, Agenesis Of Precocious puberty, male limited Pulmonary Arterial Hypertension, Hereditary Hemorrhagic Telangiectasia-Related Preeclampsia Eclampsia 4 Pseudohermaphroditism, Female, With Hypokalemia, Due To Glucocorticoid Resistance Premature Ovarian Failure 4 Progesterone Resistance Peroxisome Biogenesis Disorder, Complementation Group D Prostate Cancer, Hereditary, 9 Pediatric Obesity Prostate Cancer, Hereditary, 13 Prostate Cancer, Hereditary, 12 Plaque, Amyloid Psychomotor Agitation Peptic Ulcer Poliomyelitis Polycythemia, primary familial and congenital Personality Disorders Pemphigoid, Bullous Pain, Postoperative Paranoid Schizophrenias Persian Gulf Syndrome Pyloric Atresia Peroxisomal Disorder Phacomatosis pigmentovascularis Proximal Myopathy with Focal Depletion of Mitochondria Ppm-X Syndrome Primary Dysautonomias Premature Obstetric Labor Progressive Bulbar Palsy Paresis Pemphigus Periapical Periodontitides Pneumoconioses Polyp Pterygium Pyelonephritides Plasma Cell Granuloma, Pulmonary Polyneuropathy Pneumococcal Pneumonias Problem Behavior Pseudocholinesterase deficiency Papillomavirus Infection Pancreatitis, Alcoholic Pseudofolliculitis Barbae Pontocerebellar Hypoplasia Type 2 Polyhydramnios Paraneoplastic Syndromes Paraplegia Parapsoriases Paratuberculoses Parkinson Disease, Secondary Pemphigoid, Benign Mucous Membrane Peptic Ulcer Hemorrhage Pericarditis Peritonitis Pigmentations Pituitary Apoplexy Pneumonia, Viral Polyploidies Postherpetic Neuralgia Prenatal Exposure Delayed Effects Psychomotor Disorders Psychoses, Substance Induced Pulmonary Eosinophilia Purine-Pyrimidine Metabolism, Inborn Errors Purpura, Schoenlein Henoch Pyruvate Metabolism, Inborn Errors Post Traumatic Stress Disorders Polydipsia Porokeratosis Pancreatitis, Acute Necrotizing Prolactin Deficiency, Isolated Poisonings, Heavy Metal Pulmonary edema of mountaineers Post-Transfusion Purpura Pulmonary Hypoplasia, Primary Peanut Hypersensitivity Pentalogy, Cantrell Perinatal Death Posterior Leukoencephalopathy Syndrome Polyomavirus Infection Perivascular Epithelioid Cell Neoplasms Phyllodes Tumor of the Prostate Papillary renal cell carcinoma, sporadic Polycystic kidneys, severe infantile with tuberous sclerosis Parkinson Disease, Mitochondrial Parathyroid Adenoma, Familial Persistent Polyclonal B-Cell Lymphocytosis Pili torti developmental delay neurological abnormalities Pituitary Adenoma, Familial Isolated Ptosis, Hereditary Congenital 1 Pterygium, Antecubital Patterned dystrophy of retinal pigment epithelium Patella aplasia, coxa vara, tarsal synostosis Primary Lateral Sclerosis, Adult, 1 Palmoplantar Hyperkeratosis And True Hermaphroditism Polymicrogyria, Bilateral Occipital Prostaglandin-Endoperoxide Synthase 1 Deficiency, Platelet Pancreatic cancer, adult Pena-Shokeir syndrome type 2 Phosphoenolpyruvate carboxykinase 2 deficiency Perniola Krajewska Carnevale syndrome Paraquat lung Petty Laxova Wiedemann syndrome Pfeiffer type acrocephalosyndactyly Pericardial constriction with growth failure Papillary renal cell carcinoma, familial Plaque, Atherosclerotic Porphyria, South African type Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal Prediabetic State Pressure Ulcers Peripheral Nervous System Diseases Pseudarthroses Pulpitides Pneumocystis Pneumonia Panuveitis Parakeratoses Parapareses, Tropical Spastic Peritoneal Disease Plague Pneumonia, Staphylococcal Pneumoperitoneum Pregnancy in Diabetic Presbycuses Priapism Primary Hyperparathyroidism Paraparesis Pain, Visceral Pain, Referred Pallidopontonigral Degeneration Presenile And Senile Dementia Prehypertension Polyasplenia Periodontal Atrophy Penis agenesis Pre-Excitation Syndromes Polyposis, Gastric Paraganglioma, Extra-Adrenal Pupils, Tonic Polythelia, Familial Pelvic Organ Prolapse Panniculitides Pulmonary Heart Disease Purpuras Prolapse, Tricuspid Valve Paralyses, Vocal Cord Peroxisome Biogenesis Disorder, Complementation Group 7 Porphyria Cutanea Tarda, Type I Pain, Flank Pallor Pancreatic Pseudocyst Papilledema Paraproteinemia Parasomnias Paronychia Parotitides Partial Thromboplastin Time Periostitides Pharyngitides Phimoses Pica Pilonidal Sinus Pinealoma Plasmacytoma Platybasia Polymyalgia Rheumatica Postpartum Hemorrhage Premenstrual Syndrome Prothrombin Time Palsies, Pseudobulbar Pseudomyxoma Peritonei Pseudotumor Cerebri Pulmonary Valve Insufficiency Pulmonary Valve Stenosis Pyloric Stenosis Pyoderma Prolapse, Rectal Perforation, Retinal Pain, Shoulder Pigmentation, Skin Psychological Stresses Pleural Tuberculoses Prolapse, Uterine POEMS Syndrome Pseudopapilledema Polysomnography Papilloma, Inverted Parasitemia Pneumonia, Cryptogenic Organizing Pulmonary Atresia Pemphigus and fogo selvagem Pili Torti Pallister Killian syndrome Pancreatoblastoma Pulmonary Atresia with Intact Ventricular Septum Polyradiculoneuropathy, Chronic Inflammatory Demyelinating Purpura, Thrombocytopenic Papillary Thyroid Microcarcinoma Properdin Deficiency, Type II Properdin Deficiency, Type III Pseudohypoaldosteronism, Type IIa Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads PHACE association Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial Patchy alopecia Peroxisome Biogenesis Disorder, Complementation Group 11 Peroxisome Biogenesis Disorder, Complementation Group R Pten Hamartoma Tumor Syndrome With Granular Cell Tumor Pterygium Of Conjunctiva And Cornea Porphyria, Acute Intermittent, Nonerythroid Variant Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Polydactyly myopia syndrome Paragangliomas with Sensorineural Hearing Loss Pyelectasis Polyangiitides, Microscopic Pyloric Stenosis, Infantile Hypertrophic, 5 Porokeratosis, Disseminated Superficial Actinic, 3 Poromas Progeria Syndrome, Childhood-Onset Peri Implantitis Plasmablastic Lymphoma Parkinson Disease, Familial, Type 1 Premature Ejaculation Panencephalitides, Subacute Sclerosing Pigmented Villonodular Synovitides Pneumonia, Ventilator Associated Prieto X-linked mental retardation syndrome Parvoviridae Infections Pulmonary Alveolar Proteinosis, Acquired Plasma Cell Leukemias Pure Autonomic Failure Psychogenic Polydipsia Prolymphocytic Leukemias, B-Cell Postoperative Nausea and Vomiting Postural Orthostatic Tachycardia Syndrome Peroxisome Biogenesis Disorder, Complementation Group H Posterior column ataxia Paget's Disease, Mammary Pulmonary Blastoma Pyloric Stenosis, Infantile Hypertrophic 1 Paracoccidioidomycoses Periodontal Pocket Phobia, Social Pseudorabies Postpartum Thyroiditides Phaeohyphomycoses Pouchitis Preauricular Fistulae, Congenital Pneumonia, Idiopathic Interstitial Pericarditides, Tuberculous Pneumocephalus Polychondritides, Relapsing Preleukemia Proctitides Palindromic rheumatism Peroxisome Biogenesis Disorder, Complementation Group C Prostate Cancer, Hereditary, 7 Pdgfra-Associated Chronic Eosinophilic Leukemia Pelvic Pain Peripheral Nervous System Neoplasms Pleuropneumonia Postphlebitic Syndrome Prognathism Pseudotumor, Orbital Pseudolymphoma Papillomatosis, Familial Cutaneous Postthrombotic Syndrome Post-Concussion Syndrome Posterior Tibial Tendon Dysfunction Peripheral Cone Dystrophy Parkinson Disease 12 Peroxisome Biogenesis Disorder, Complementation Group 1 Pulmonary Aspergillosis Primary cortisol resistance Prinzmetal's variant angina Prodromal Symptom Psittacoses Paragonimiases Parkinson Disease, Postencephalitic Peptic Ulcer Perforation Perceptual Disorder Picornaviridae Infections Pinta Pityriasis Rosea Poland Syndrome Polyradiculopathy Polyradiculoneuropathies Postpericardiotomy Syndrome Poxviridae Infections Pregnancies, Tubal Presbyopia Proctocolitis Prurigo Pruritus Ani Psychophysiologic Disorders Psychoses, Alcoholic Pyelocystitis Pyelonephritides, Xanthogranulomatous Pyometra Pyonephrosis Phenomenon, Shwartzman Pinguecula Pityriasis Lichenoides Periodontal Attachment Loss Pestivirus Infections Pneumovirus Infections Papilloma, Intraductal Prosopagnosia Phobia, Specific Prostatism Placenta, Retained Persistent Vegetative State Pili annulati Perifolliculitis Capitis Abscedens Et Suffodiens, Familial Pyogenic Liver Abscess Previa, Vasa Paraneoplastic Polyneuropathies Perforations, Spontaneous Pseudoainhum Patent Ductus Venosus Pulmonary Atresia With Ventricular Septal Defect Pseudoaminopterin syndrome Pains, Breakthrough Pseudo-Zellweger syndrome Primary Headache Disorders Pyomyositis Prostate Cancer, Hereditary, 4 Pick Complex Progressive Familial Heart Block, Type II Parkinson Disease 10 Pericardial Effusion, Chronic Pachygyria, frontotemporal Pseudoarylsulfatase A Deficiency Progressive Encephalomyelitis with Rigidity Peroxisome Biogenesis Disorder, Complementation Group G Pierre Robin sequence with pectus excavatum and rib and scapular anomalies Peroxisome Biogenesis Disorder, Complementation Group 3 Pseudoxanthoma Elasticum, Heterozygous Porokeratosis punctata palmaris et plantaris Polyposis Of Gastric Fundus Without Polyposis Coli Platelet Aggregation, Spontaneous Pancreatitis, Calcific Pancreatitis, Graft Protein C Deficiency, Acquired Polymicrogyria, Asymmetric Parkinson Disease 16 Primary angiitis of the central nervous system Paranasal sinus teratocarcinosarcoma (type) Pseudoangiomatous stromal hyperplasia Pancreatic islet cell tumors Polycystic kidney disease, type 1 Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections Prosopagnosia, hereditary Plasmacytoma anaplastic Plexosarcoma Psychological Trauma Pdgfrb-Associated Chronic Eosinophilic Leukemia Pancreas Patella Periodontium Peritoneum Pharynx Phenotype Pleura Pons Point Mutation Palate Peroxisome Posture Pseudoinflammatory fundus dystrophy