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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   |