Disease Name Symbol Acronym
Pa Polymorphism of Alpha-2-Globulin PPL057
Pachydermodactyly, Familial PCH021
Pachygyria PCH002
Pachygyria with Mental Retardation, Seizures, and Arachnoid Cysts PCH018
Pachygyria-Intellectual Disability-Epilepsy Syndrome PCH017
Pachygyria, Frontotemporal PCH004
Pachyonychia Congenita 1 PCH015
Pachyonychia Congenita 2 PCH012
Pachyonychia Congenita 3 PCH010
Pachyonychia Congenita 4 PCH011
Pachyonychia Congenita, Autosomal Recessive PCH020
Pacinian Tumor PCN001
Pacman Dysplasia PCM001
Pacs1-Related Syndrome PCS002
Paget Disease of Bone 2, Early-Onset PGT009
Paget Disease of Bone 3 PGT007
Paget Disease of Bone 4 PGT006
Paget Disease of Bone 5, Juvenile-Onset PGT008
Paget Disease of Bone 6 PGT011
Paget Disease, Extramammary PGT003
Paget's Disease of Bone PGT001
Pagod Syndrome PGD001
Pagon Stephan Syndrome PGN001
Pain Agnosia PNG002
Paine Syndrome PNS012
Painful Legs and Moving Toes Syndrome PNF002
Painful Orbital and Systemic Neurofibromas-Marfanoid Habitus Syndrome PNF001
Palant Cleft Palate Syndrome PLN009
Palatopharyngeal Incompetence PLT007
Palindromic Rheumatism PLN005
Pallidal Degeneration, Progressive, with Retinitis Pigmentosa PLL015
Pallister W Syndrome PLL004
Pallister-Hall Syndrome PLL001
Pallister-Killian Mosaic Syndrome PLL005
Pallister-Killian Syndrome PLL008
Palmaris Longus Muscle, Absence of PLM161
Palmer Pagon Syndrome PLM045
Palmomental Reflex PLM162
Palmoplantar Carcinoma, Multiple Self-Healing PLM156
Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal PLM173
Palmoplantar Keratoderma and Congenital Alopecia 1 PLM158 PPKCA1
Palmoplantar Keratoderma and Congenital Alopecia 2 PLM149
Palmoplantar Keratoderma and Woolly Hair PLM137
Palmoplantar Keratoderma I, Striate, Focal, or Diffuse PLM160
Palmoplantar Keratoderma of Sybert PLM046
Palmoplantar Keratoderma-Sclerodactyly Syndrome PLM113
Palmoplantar Keratoderma, Bothnian Type PLM135
Palmoplantar Keratoderma, Epidermolytic PLM102
Palmoplantar Keratoderma, Mutilating, with Periorificial Keratotic Plaques PLM100
Palmoplantar Keratoderma, Mutilating, with Periorificial Keratotic Plaques, X-Linked PLM172
Palmoplantar Keratoderma, Nagashima Type PLM104
Palmoplantar Keratoderma, Nonepidermolytic PLM136
Palmoplantar Keratoderma, Nonepidermolytic, Focal 1 PLM174
Palmoplantar Keratoderma, Nonepidermolytic, Focal 2 PLM142
Palmoplantar Keratoderma, Nonepidermolytic, Focal or Diffuse PLM131
Palmoplantar Keratoderma, Norrbotten Recessive Type PLM154
Palmoplantar Keratoderma, Punctate Type Ia PLM159
Palmoplantar Keratoderma, Punctate Type Ib PLM176
Palmoplantar Keratoderma, Punctate Type Ii PLM163
Palmoplantar Keratoderma, Punctate Type Iii PLM152 AKE
Palmoplantar Keratosis PLM029
Panbronchiolitis, Diffuse PNB004
Pancreas Adenocarcinoma PNC033
Pancreas Disease PNC034
Pancreas Lymphoma PNC007
Pancreas Sarcoma PNC009
Pancreas, Annular PNC118
Pancreas, Dorsal, Agenesis of PNC120
Pancreatic Acinar Cell Adenocarcinoma PNC015
Pancreatic Acth Hormone Producing Tumor PNC029
Pancreatic Adenoma PNC049
Pancreatic Agenesis PNC045
Pancreatic Agenesis 1 PNC106
Pancreatic Agenesis 2 PNC105
Pancreatic and Cerebellar Agenesis PNC104
Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus PNC050
Pancreatic Cancer PNC035
Pancreatic Cancer 1 PNC094
Pancreatic Cancer 2 PNC111
Pancreatic Cancer 3 PNC095
Pancreatic Cancer 4 PNC103
Pancreatic Cancer, Childhood PNC051
Pancreatic Cholera PNC016
Pancreatic Colloid Cystadenocarcinoma PNC037
Pancreatic Colloid Cystadenoma PNC024
Pancreatic Cystadenocarcinoma PNC038
Pancreatic Cystadenoma PNC039
Pancreatic Delta Cell Neoplasm PNC040
Pancreatic Ductal Adenocarcinoma PNC041
Pancreatic Ductal Carcinoma PNC013
Pancreatic Endocrine Carcinoma PNC008
Pancreatic Foamy Gland Adenocarcinoma PNC031
Pancreatic Gastrinoma PNC027
Pancreatic Insufficiency, Combined Exocrine PNC123
Pancreatic Intraductal Papillary-Colloid Carcinoma PNC042
Pancreatic Intraductal Papillary-Mucinous Adenoma PNC022
Pancreatic Intraductal Papillary-Mucinous Neoplasm PNC043
Pancreatic Invasive Intraductal Papillary-Mucinous Carcinoma PNC021
Pancreatic Invasive Mucinous Cystadenocarcinoma PNC003
Pancreatic Lipase Deficiency PNC048
Pancreatic Lipomatosis Duodenal Stenosis PNC054
Pancreatic Lymphoma, Familial PNC125
Pancreatic Mucinous Cystadenoma PNC002
Pancreatic Mucinous Ductal Ectasia PNC026
Pancreatic Neuroendocrine Tumor PNC119
Pancreatic Non-Functioning Delta Cell Tumor PNC023
Pancreatic Non-Invasive Intraductal Papillary-Mucinous Carcinoma PNC030
Pancreatic Non-Invasive Mucinous Cystadenocarcinoma PNC004
Pancreatic Serous Cystadenocarcinoma PNC014
Pancreatic Serous Cystadenoma PNC018
Pancreatic Serous Cystic Neoplasm PNC017
Pancreatic Signet Ring Cell Adenocarcinoma PNC010
Pancreatic Solid Pseudopapillary Carcinoma PNC020
Pancreatic Somatostatinoma PNC006
Pancreatic Steatorrhea PNC028
Pancreatic Vasoactive Intestinal Peptide Producing Tumor PNC011
Pancreatitis PNC044
Pancreatitis, Hereditary PNC108
Pancreatitis, Pediatric PNC055
Pancreatitis, Sclerosing Cholangitis, and Sicca Complex PNC124
Pancreatoblastoma PNC019
Pancytopenia PNC001
Pancytopenia and Occlusive Vascular Disease PNC121
Pandas PND004
Panencephalitis, Subacute Sclerosing PNN005
Panhypophysitis PNH004
Panhypopituitarism, X-Linked PNH005
Panic Disorder PNC025
Panic Disorder 1 PNC122
Panic Disorder 2 PNC070
Panic Disorder 3 PNC068
Panner Disease PNN003
Panniculitis PNN001
Panniculitis-Induced Localized Lipodystrophy PNN006
Panophthalmitis PNP001
Panostotic Fibrous Dysplasia PNS013
Panuveitis PNV001
Papillary Adenocarcinoma PPL018
Papillary Adenofibroma PPL016
Papillary Adenoma PPL001
Papillary Carcinoma PPL002
Papillary Carcinoma of the Cervix Uteri PPL043
Papillary Carcinoma of the Corpus Uteri PPL042
Papillary Conjunctivitis PPL019
Papillary Craniopharyngioma PPL009
Papillary Cystadenocarcinoma PPL003
Papillary Ependymoma PPL013
Papillary Extrahepatic Bile Duct Adenocarcinoma PPL008
Papillary Follicular Thyroid Adenocarcinoma PPL010
Papillary Glioneuronal Tumors PPL060
Papillary Hidradenoma PPL017
Papillary Meningioma of the Cerebellum PPL011
Papillary Pattern Testicular Yolk Sac Tumor PPL012
Papillary Serous Adenocarcinoma PPL007
Papillary Squamous Carcinoma PPL004
Papillary Thymic Adenocarcinoma PPL015
Papillary Thyroid Microcarcinoma PPL035
Papillary Transitional Carcinoma PPL014
Papillary Tumor of the Pineal Region PPL050
Papilledema PPL021
Papilloma PPL022
Papilloma of Choroid Plexus PPL058
Papillomatosis, Confluent and Reticulated PPL052
Papillomatosis, Florid, of Nipple PPL053
Papillon-Lefevre Syndrome PPL049
Papillorenal Syndrome PPL048 PAPRS
Papular Elastorrhexis PPL044
Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome PPL061
Papular Mucinosis PPL026
Papular Mucinosis of Infancy PPL045
Papular Urticaria PPL027
Papular Xanthoma PPL038
Paracetamol Poisoning PRC051
Parachordoma PRC011
Parachute Tricuspid Valve PRC042
Paracoccidioidomycosis PRC002
Paraganglioma PRG013
Paraganglioma and Gastric Stromal Sarcoma PRG017
Paragangliomas 1 PRG018
Paragangliomas 2 PRG019
Paragangliomas 3 PRG020
Paragangliomas 4 PRG021 PGL4
Paragangliomas 5 PRG094
Paragonimiasis PRG008
Parainfluenza Virus Type 3 PRN029
Paralysis Agitans, Juvenile, of Hunt PRL020
Paralytic Ileus PRL008
Paralytic Lagophthalmos PRL006
Paralytic Poliomyelitis PRL013
Paralytic Squint PRL014
Parameningeal Embryonal Rhabdomyosarcoma PRM208
Parametritis PRM008
Parametrium Malignant Neoplasm PRM017
Paramolar Tubercle of Bolk PRM289
Paramyloidosis PRM123
Paramyotonia Congenita of Von Eulenburg PRM057
Parana Hard-Skin Syndrome PRN056
Paranasal Sinus Cancer PRN020
Paranasal Sinus Cancer, Adult PRN030
Paranasal Sinus Cancer, Childhood PRN031
Paranasal Sinus Disease PRN021
Paranasal Sinus Lymphoma PRN002
Paranasal Sinus Sarcoma PRN003
Paraneoplastic Cerebellar Degeneration PRN032
Paraneoplastic Neurologic Disorders PRN033
Paraneoplastic Pemphigus PRN049
Paraneoplastic Polyneuropathy PRN018
Paraneoplastic Syndromes PRN039
Paraneoplastic Uveitis PRN060
Paranoid Personality Disorder PRN010
Paranoid Schizophrenia PRN009
Paraomphalocele PRM033
Paraparetic Variant of Guillain-Barré Syndrome PRP073
Parapharyngeal Meningioma PRP008
Paraphilia Disorder PRP015
Paraphimosis PRP013
Paraplegia PRP016
Parapsoriasis PRP005
Paraquat Lung PRQ001
Paraquat Poisoning PRQ002
Parasagittal Meningioma PRS024
Parasitic Conjunctivitis PRS026
Parasitic Ectoparasitic Infectious Disease PRS033
Parasitic Eyelid Infestation PRS018
Parasitic Helminthiasis Infectious Disease PRS034
Parasitic Ichthyosporea Infectious Disease PRS035
Parasitic Protozoa Infectious Disease PRS036
Parasomnia, Sleep Bruxism Type PRS132
Parasomnia, Sleepwalking Type PRS118
Parastremmatic Dwarfism PRS051
Paratesticular Adenocarcinoma PRT095
Paratesticular Lipoma PRT028
Parathyroid Adenoma PRT029
Parathyroid Cancer, Childhood PRT046
Parathyroid Carcinoma PRT010
Parathyroid Gland Disease PRT030
Parathyroid Oncocytic Adenoma PRT020
Parathyroid Transitional Clear Cell Adenoma PRT021
Paratyphoid Fever PRT002
Paraurethral Gland Cancer PRR005
Parc Syndrome PRC021
Parenchymatous Neurosyphilis PRN006
Paresthesia PRS063
Parietal Encephalocele PRT087
Parietal Foramina PRT042
Parietal Foramina 1 PRT059
Parietal Foramina 2 PRT060
Parietal Foramina 3 PRT113
Parietal Foramina with Cleidocranial Dysplasia PRT043
Parietal Lobe Ependymoma PRT099
Parietal Lobe Neoplasm PRT023
Parkes Weber Syndrome PRK003
Parkin Type of Early-Onset Parkinson Disease PRK046
Parkinson Disease 1, Autosomal Dominant PRK085
Parkinson Disease 10 PRK025
Parkinson Disease 11, Autosomal Dominant PRK094
Parkinson Disease 12 PRK022
Parkinson Disease 13, Autosomal Dominant PRK096
Parkinson Disease 14, Autosomal Recessive PRK071
Parkinson Disease 15, Autosomal Recessive Early-Onset PRK086
Parkinson Disease 16 PRK058
Parkinson Disease 17 PRK052
Parkinson Disease 18, Autosomal Dominant PRK099
Parkinson Disease 19a, Juvenile-Onset PRK081
Parkinson Disease 2, Autosomal Recessive Juvenile PRK089
Parkinson Disease 20, Early-Onset PRK065
Parkinson Disease 21 PRK070
Parkinson Disease 22, Autosomal Dominant PRK083
Parkinson Disease 23, Autosomal Recessive Early-Onset PRK100
Parkinson Disease 3, Autosomal Dominant PRK090
Parkinson Disease 4, Autosomal Dominant PRK091
Parkinson Disease 5, Autosomal Dominant PRK098
Parkinson Disease 6, Autosomal Recessive Early-Onset PRK092
Parkinson Disease 7, Autosomal Recessive Early-Onset PRK021
Parkinson Disease 8, Autosomal Dominant PRK093
Parkinson Disease Type 9 PRK008
Parkinson Disease, Late-Onset PRK057
Parkinson Disease, Mitochondrial PRK088
Parkinson-Dementia Syndrome PRK087
Parkinsonism with Dementia of Guadeloupe PRK050
Parkinsonism with Spasticity, X-Linked PRK066
Parkinsonism-Dystonia, Infantile PRK069
Paronychia PRN014
Parotid Disease PRT031
Parotid Gland Adenoid Cystic Carcinoma PRT100
Parotid Gland Cancer PRT009
Parotid Salivary Glands, Polycystic Dysgenetic Disease of PRT122
Parotidomegaly, Hereditary Bilateral PRT116
Parotitis PRT026
Parotitis, Juvenile Recurrent PRT125
Parovarian Cyst PRV001
Paroxysmal Choreoathetosis PRX022
Paroxysmal Cold Hemoglobinuria PRX008
Paroxysmal Exertion-Induced Dyskinesia PRX086
Paroxysmal Extreme Pain Disorder PRX015
Paroxysmal Hemicrania PRX009
Paroxysmal Nocturnal Hemoglobinuria PRX003
Paroxysmal Nocturnal Hemoglobinuria 1 PRX094
Paroxysmal Nocturnal Hemoglobinuria 2 PRX067
Paroxysmal Nonkinesigenic Dyskinesia 1 PRX088 DYT8
Paroxysmal Nonkinesigenic Dyskinesia 2 PRX024
Paroxysmal Nonkinesigenic Dyskinesia, 3, with or Without Generalized Epilepsy PRX090
Paroxysmal Tonic Upgaze, Benign Childhood, with Ataxia PRX084
Paroxysmal Ventricular Fibrillation PRX010
Paroxysomal Nonkinesigenic Dyskinesia PRX087
Pars Planitis PRS012
Parsonage Turner Syndrome PRS053
Partial Arterial Retinal Occlusion PRT027
Partial Atrioventricular Canal PRT048
Partial Central Choroid Dystrophy PRT032
Partial Circumpapillary Choroid Dystrophy PRT016
Partial Corpus Callosum Agenesis-Cerebellar Vermis Hypoplasia with Posterior Fossa Cysts Syndrome PRT098
Partial Cryptophthalmia PRT091
Partial Deep Dermal and Full Thickness Burns PRT089
Partial Deletion of Y PRT049
Partial Duplication of the Short Arm of Chromosome X PRT106
Partial Fetal Alcohol Syndrome PRT001
Partial Hydatidiform Mole PRT086
Partial Lipodystrophy PRT078
Partial Lipodystrophy, Congenital Cataracts, and Neurodegeneration Syndrome PRT097
Partial Motor Epilepsy PRT006
Partial of Retinal Vein Occlusion PRT007
Partial Optic Atrophy PRT024
Partial Sensory Epilepsy PRT004
Partial Septate Uterus PRT111
Partial Third-Nerve Palsy PRT015
Partial Trisomy Distal 4q PRT131
Partially Involuting Congenital Hemangioma PRT109
Partington X-Linked Mental Retardation Syndrome PRT052
Partington-Anderson Syndrome PRT120
Parvovirus Antenatal Infection PRV008
Passos-Bueno Syndrome PSS001
Passovoy Factor Defect PSS004
Pasteurella Multocida Infection PST037
Pasteurellosis PST010
Patau Syndrome PTS001
Patau Syndrome Trisomy 13 PTS019
Patel Bixler Syndrome PTL005
Patella Aplasia-Hypoplasia PTL010
Patella, Chondromalacia of PTL009
Patella, Familial Recurrent Dislocation of PTL011
Patellar Tendinitis PTL003
Patellofemoral Pain Syndrome PTL002
Patent Ductus Arteriosus 1 PTN014
Patent Ductus Arteriosus 2 PTN013
Patent Ductus Arteriosus 3 PTN012
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies PTN011
Patent Ductus Venosus PTN004
Patent Foramen Ovale PTN001
Patent Urachus PTN009
Paternal 20q13.2q13.3 Microdeletion Syndrome PTR014
Paternal Uniparental Disomy of Chromosome 1 PTR011
Paternal Uniparental Disomy of Chromosome 13 PTR023
Paternal Uniparental Disomy of Chromosome 20 PTR020
Paternal Uniparental Disomy of Chromosome 21 PTR021
Paternal Uniparental Disomy of Chromosome 5 PTR019
Paternal Uniparental Disomy of Chromosome 6 PTR018
Paternal Uniparental Disomy of Chromosome 7 PTR022
Paternal Uniparental Disomy of Chromosome X PTR015
Pathologic Nystagmus PTH003
Pathological Gambling PTH002
Patterned Macular Dystrophy PTT054
Patterson Pseudoleprechaunism Syndrome PTT016
Patulous Eustachian Tube PTL001
Pauci-Immune Glomerulonephritis PCM002
Pauci-Immune Glomerulonephritis with Anca PCM004
Pauci-Immune Glomerulonephritis Without Anca PCM003
Pauciarticular Chronic Arthritis PCR001
Pauciarticular Onset Juvenile Idiopathic Arthritis PCR003
Pax2-Related Disorder PX2001
Pcdh19-Related Female-Limited Epilepsy PCD002
Pdgfra-Associated Chronic Eosinophilic Leukemia PDG001
Pdgfrb-Associated Chronic Eosinophilic Leukemia PDG002
Peach Allergy PCH016
Peanut Allergy PNT038
Pearson Marrow-Pancreas Syndrome PRS127
Pechet Factor Deficiency PCH019
Pectus Carinatum PCT001
Pectus Excavatum PCT003
Pectus Excavatum, Macrocephaly, Short Stature, and Dysplastic Nails PCT002
Pediatric Acute-Onset Neuropsychiatric Syndrome PDT043
Pediatric Angiosarcoma PDT004
Pediatric Arterial Ischemic Stroke PDT041
Pediatric Castleman Disease PDT039
Pediatric Cerebral Ependymoblastoma PDT012
Pediatric Cns Choriocarcinoma PDT011
Pediatric Cns Embryonal Cell Carcinoma PDT006
Pediatric Collagenous Gastritis PDT044
Pediatric Ependymoma PDT014
Pediatric Epithelioid Sarcoma PDT008
Pediatric Extraocular Retinoblastoma PDT013
Pediatric Fibrosarcoma PDT019
Pediatric Germ Cell Cancer PDT020
Pediatric Hypertension PDT040
Pediatric Infratentorial Ependymoblastoma PDT017
Pediatric Infratentorial Ependymoma PDT016
Pediatric Intraocular Retinoblastoma PDT010
Pediatric Leptomeningeal Melanoma PDT007
Pediatric Liposarcoma PDT009
Pediatric Lymphoma PDT001
Pediatric Meningioma PDT002
Pediatric Mesenchymal Chondrosarcoma PDT005
Pediatric Multiple Sclerosis PDT025
Pediatric Myxoid Chondrosarcoma PDT018
Pediatric Osteosarcoma PDT021
Pediatric Ovarian Dysgerminoma PDT003
Pediatric Ovarian Germ Cell Tumor PDT022
Pediatric Supratentorial Ependymoma PDT015
Pediatric Systemic Lupus Erythematosus PDT035
Pediatric T-Cell Leukemia PDT026
Pediatric Testicular Germ Cell Tumor PDT023
Pediatric Ulcerative Colitis PDT027
Pediculus Humanus Capitis Infestation PDC002
Pediculus Humanus Corporis Infestation PDC003
Pedophilia PDP001
Peeling Skin Syndrome PLN008
Peeling Skin Syndrome 1 PLN017
Peeling Skin Syndrome 2 PLN018
Peeling Skin Syndrome 3 PLN021
Peeling Skin Syndrome 4 PLN024
Peeling Skin Syndrome 5 PLN025
Peeling Skin Syndrome Type C PLN027
Peeling Skin with Leukonychia, Acral Punctate Keratoses, Cheilitis, and Knuckle Pads PLN020
Peho Syndrome PHS005
Peho-Like Syndrome PHL010
Pelger-Huet Anomaly PLG001
Pelger-Huet-Like Anomaly and Episodic Fever with Abdominal Pain PLG009
Peliosis Hepatis PLS002
Pelizaeus-Merzbacher Disease PLZ001
Pelizaeus-Merzbacher Disease in Female Carriers PLZ009
Pelizaeus-Merzbacher Disease, Classic Form PLZ007
Pelizaeus-Merzbacher Disease, Transitional Form PLZ008
Pelizaeus-Merzbacher-Like Disease PLZ002
Pellagra PLL002
Pellagra-Like Syndrome PLL014
Pellucid Marginal Degeneration PLL009
Pelvic Dysplasia Arthrogryposis of Lower Limbs PLV006
Pelvic Hypoplasia with Lower-Limb Arthrogryposis PLV018
Pelvic Inflammatory Disease PLV003
Pelvic Lipomatosis PLV001
Pelvic Lipomatosis with Crossed Renal Ectopia PLV019
Pelvic Muscle Wasting PLV002
Pelvic Organ Prolapse PLV020
Pelvic Organ Prolapse 2 PLV014
Pelvic Varices PLV004
Pelvis-Shoulder Dysplasia PLV015
Pemphigoid Gestationis PMP002
Pemphigus PMP001
Pemphigus and Fogo Selvagem PMP003
Pemphigus Erythematosus PMP009
Pemphigus Foliaceus PMP004
Pemphigus Vegetans PMP008
Pemphigus Vulgaris PMP005
Pemphigus Vulgaris, Familial PMP006
Pendred Syndrome PND002
Pendred Syndrome/nonsyndromic Enlarged Vestibular Aqueduct PND005
Penicillin Allergy PNC085
Penicilliosis PNC005
Penile Agenesis PNL023
Penile Cancer PNL012
Penile Cancer, Adult PNL017
Penile Cancer, Childhood PNL018
Penile Disease PNL013
Penile Urethral Cancer PNL006
Penis Agenesis PNS014
Penis Basal Cell Carcinoma PNS008
Penis Basaloid Carcinoma PNS003
Penis Carcinoma in Situ PNS002
Penis Mixed Squamous Cell Carcinoma PNS005
Penis Non-Invasive Verrucous Carcinoma PNS001
Penis Paget's Disease PNS004
Penis Papillary Carcinoma PNS006
Penis Sarcoma PNS007
Penis Squamous Cell Carcinoma PNS010
Penis Verrucous Carcinoma PNS011
Penoscrotal Transposition PNS015
Pentalogy of Cantrell PNT005
Pentosuria PNT006
Penttinen-Aula Syndrome PNT007
Pepck 1 Deficiency PPC001
Peptic Esophagitis PPT001
Peptic Ulcer Disease PPT005
Peptic Ulcer Perforation PPT002
Peptidic Growth Factors Deficiency PPT004
Perforated Corneal Ulcer PRF002
Perforation of Bile Duct PRF001
Peri-Anal Fistula PRN051
Periampullary Adenocarcinoma PRM014
Periampullary Adenoma PRM190
Perianal Hematoma PRN017
Perianal Skin Paget's Disease PRN012
Periapical Granuloma PRP002
Periapical Periodontitis PRP017
Periarthritis PRR001
Pericardial and Diaphragmatic Defect PRC041
Pericardial Effusion PRC012
Pericardial Effusion, Chronic PRC052
Pericardial Mesothelioma PRC010
Pericardial Tuberculosis PRC005
Pericarditis PRC013
Pericardium Cancer PRC014
Pericardium Leiomyoma PRC006
Pericholangitis PRC008
Perichondritis of Auricle PRC015
Pericoronitis PRC001
Periductal Breast Myoepitheliosis PRD005
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial PRF005
Perilymphatic Fistula PRL021
Perimyositis PRM034
Perinatal Intestinal Perforation PRN015
Perinatal Jaundice Due to Hepatocellular Damage PRN005
Perinatal Necrotizing Enterocolitis PRN019
Perineocele PRN004
Perinephritis PRN007
Perineural Angioma PRN013
Perineurioma PRN022
Periocular Meningioma PRC007
Periodic Fever, Aphthous Stomatitis, Pharyngitis and Adenitis PRD012
Periodic Fever, Familial, Autosomal Dominant PRD013
Periodic Fever, Menstrual Cycle-Dependent PRD041
Periodic Limb Movement Disorder PRD002
Periodic Paralyses PRD017
Periodic Paralysis with Later-Onset Distal Motor Neuropathy PRD033
Periodic Paralysis with Transient Compartment-Like Syndrome PRD032
Periodontal Disease PRD007
Periodontal Ehlers-Danlos Syndrome PRD037
Periodontitis PRD008
Periodontitis, Aggressive, 1 PRD039
Periodontitis, Aggressive, 2 PRD018
Periodontitis, Chronic PRD040
Periodontosis PRD003
Perioral Myoclonia with Absences PRR019
Periosteal Chondrosarcoma PRS016
Periosteal Osteogenic Sarcoma PRS029
Periostitis PRS037
Peripapillary Atrophy, Beta Type PRP100
Peripartum Cardiomyopathy PRP009
Peripheral Arterial Occlusive Disease 1 PRP050
Peripheral Artery Disease PRP080
Peripheral Cone Dystrophy PRP099
Peripheral Degeneration of Cornea PRP014
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease PRP066
Peripheral Dysostosis PRP090
Peripheral Epithelioid Sarcoma PRP006
Peripheral Focal Chorioretinitis PRP012
Peripheral Nerve Schwannoma PRP018
Peripheral Nervous System Disease PRP019
Peripheral Nervous System Ganglioneuroblastoma PRP020
Peripheral Nervous System Neoplasm PRP021
Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain PRP096
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss PRP075
Peripheral Osteosarcoma PRP024
Peripheral Pulmonary Stenosis PRP101
Peripheral Resistance to Thyroid Hormones PRP074
Peripheral Retinal Degeneration PRP026
Peripheral Scars of Retina PRP004
Peripheral T-Cell Lymphoma PRP036
Peripheral Vascular Disease PRP027
Peripheral Vertigo PRP028
Peritoneal Benign Neoplasm PRT033
Peritoneal Cystic Mesothelioma PRT085
Peritoneal Mesothelioma PRT096
Peritoneal Serous Adenocarcinoma PRT034
Peritoneal Serous Papillary Adenocarcinoma PRT017
Peritoneum Cancer PRT035
Peritonitis PRT036
Perivascular Epithelioid Cell Tumor PRV003
Periventricular Heterotopia with Microcephaly, Autosomal Recessive PRV020
Periventricular Leukomalacia PRV004
Periventricular Nodular Heterotopia PRV002
Periventricular Nodular Heterotopia 1 PRV019
Periventricular Nodular Heterotopia 6 PRV016
Periventricular Nodular Heterotopia 7 PRV018
Perlman Syndrome PRL032
Permanent Molars, Secondary Retention of PRM288
Pernicious Anemia PRN011
Perniosis PRN035
Peroneal Nerve Paralysis PRN008
Peroneal Nerve, Accessory Deep PRN063
Peroneal Neuropathy PRN016
Peroneus Tertius Muscle, Absence of PRN065
Peroxidase, Salivary PRX092
Peroxisomal Acyl-Coa Oxidase Deficiency PRX028
Peroxisomal Beta-Oxidation Disorder PRX076
Peroxisomal Biogenesis Disorders PRX077
Peroxisomal Disease PRX001
Peroxisomal Fatty Acyl-Coa Reductase 1 Disorder PRX072
Peroxisome Biogenesis Disorder 10a PRX048
Peroxisome Biogenesis Disorder 10b PRX089
Peroxisome Biogenesis Disorder 11a PRX055
Peroxisome Biogenesis Disorder 11b PRX056
Peroxisome Biogenesis Disorder 12a PRX054
Peroxisome Biogenesis Disorder 13a PRX052
Peroxisome Biogenesis Disorder 14b PRX053
Peroxisome Biogenesis Disorder 1a PRX059
Peroxisome Biogenesis Disorder 1b PRX045
Peroxisome Biogenesis Disorder 2a PRX063
Peroxisome Biogenesis Disorder 2b PRX064
Peroxisome Biogenesis Disorder 3a PRX065
Peroxisome Biogenesis Disorder 3b PRX066
Peroxisome Biogenesis Disorder 4a PRX057
Peroxisome Biogenesis Disorder 4b PRX058
Peroxisome Biogenesis Disorder 5a PRX060
Peroxisome Biogenesis Disorder 5b PRX047
Peroxisome Biogenesis Disorder 6a PRX051
Peroxisome Biogenesis Disorder 6b PRX043
Peroxisome Biogenesis Disorder 7a PRX046
Peroxisome Biogenesis Disorder 7b PRX068
Peroxisome Biogenesis Disorder 8a PRX091
Peroxisome Biogenesis Disorder 8b PRX062
Peroxisome Biogenesis Disorder 9b PRX050
Peroxisome Biogenesis Disorder-Zellweger Syndrome Spectrum PRX096
Peroxisome Disorders PRX034
Perrault Syndrome PRR025
Perrault Syndrome 1 PRR020
Perrault Syndrome 2 PRR022
Perrault Syndrome 3 PRR024
Perrault Syndrome 4 PRR021
Perrault Syndrome 5 PRR026
Perrault Syndrome 6 PRR033
Perry Syndrome PRR007
Persian Gulf Syndrome PRS011
Persistent Eustachian Valve PRS112
Persistent Fetal Circulation Syndrome PRS030
Persistent Fifth Aortic Arch PRS111
Persistent Generalized Lymphadenopathy PRS123
Persistent Genital Arousal Disorder PRS119
Persistent Hyperplastic Primary Vitreous PRS062
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant PRS137
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive PRS122
Persistent Idiopathic Facial Pain PRS120
Persistent Left Superior Vena Cava Connecting to the Left-Sided Atrium PRS113
Persistent Mullerian Duct Syndrome PRS049
Persistent Mullerian Duct Syndrome, Types I and Ii PRS128
Persistent Placoid Maculopathy PRS110
Persistent Polyclonal B-Cell Lymphocytosis PRS108
Persistent Vegetative State PRS064
Personality Disorder PRS038
Pertussis PRT037
Pervasive Developmental Disorder PRV006
Pes Anserinus Tendinitis or Bursitis PSN001
Peters Anomaly-Cataract Syndrome PTR027
Peters-Plus Syndrome PTR032
Petit-Fryns Syndrome PTT018
Petroclival Meningioma PTR002
Petrositis PTR001
Petrous Apex Meningioma PTR003
Pettigrew Syndrome PTT059
Peutz-Jeghers Syndrome PTZ001
Peyronie Disease PYR039
Peyronie's Disease PYR010
Pfeiffer Kapferer Syndrome PFF002
Pfeiffer Mayer Syndrome PFF003
Pfeiffer Rockelein Syndrome PFF005
Pfeiffer Syndrome PFF001 PS
Pfeiffer Tietze Welte Syndrome PFF006
Pfeiffer-Palm-Teller Syndrome PFF010
Pgm3-Cdg PGM026
Phace Association PHC018
Phace Syndrome PHC004
Phacoanaphylactic Uveitis PHC015
Phacogenic Glaucoma PHC002
Phacolytic Glaucoma PHC001
Phacomatosis Pigmentokeratotica PHC005
Phacomatosis Pigmentovascularis PHC006
Phaeochromocytoma PHC013
Phaeohyphomycosis PHH001
Phagocyte Bactericidal Dysfunction PHG002
Phagocytosis, Plasma-Related Defect in PHG003
Phakomatosis Cesioflammea PHK008
Phakomatosis Cesiomarmorata PHK009
Phakomatosis Pigmentokeratotica PHK006
Phakomatosis Spilorosea PHK010
Phalangeal Microgeodic Syndrome PHL009
Phalanx Chondroma PHL011
Pharyngeal-Cervical-Brachial Variant of Guillain-Barré Syndrome PHR007
Pharyngitis PHR003
Pharyngoconjunctival Fever PHR002
Pharynx Cancer PHR004
Pharynx Carcinoma in Situ PHR001
Phaver Syndrome PHV001
Phelan-Mcdermid Syndrome PHL006
Phencyclidine Abuse PHN001
Phenformin 4-Hydroxylation PHN014
Phenobarbital Antenatal Exposure PHN013
Phenylketonuria PHN003
Phenytoin or Carbamazepine Toxicity PHN012
Phenytoin Toxicity PHN011
Pheochromocytoma PHC003
Pheochromocytoma--Islet Cell Tumor Syndrome PHC017
Pheochromocytoma, Childhood PHC007
Philadelphia-Negative Chronic Myeloid Leukemia PHL007
Philophthalmiasis PHL002
Phimosis PHM001
Phip-Related Disorder PHP001
Phlebectasia of Lips PHL012
Phlebotomus Fever PHL003
Phlegmonous Dacryocystitis PHL004
Phlyctenulosis PHL001
Phobia, Specific PHB003
Phobic Disorder PHB001
Phocomelia PHC014
Phocomelia Ectrodactyly Deafness Sinus Arrhythmia PHC009
Phocomelia-Ectrodactyly, Ear Malformation, Deafness, and Sinus Arrhythmia PHC016
Phonagnosia PHN002
Phosphatase, Acid, of Tissues PHS025
Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic PHS029
Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial PHS028
Phosphoglucomutase 4 PHS026
Phosphoglycerate Dehydrogenase Deficiency PHS021
Phosphoglycerate Kinase 1 Deficiency PHS014
Phosphoglycerate Kinase Deficiency PHS009
Phosphoglycerate Mutase Deficiency PHS010
Phosphoglycoprotein 1 PHS027
Phosphohydroxylysinuria PHS019
Phosphomannoisomerase Deficiency PHS011
Phosphoribosylpyrophosphate Synthetase Deficiency PHS012
Phosphoribosylpyrophosphate Synthetase Superactivity PHS004
Phosphorus Metabolism Disease PHS001
Phosphorylase Kinase Deficiency PHS018
Phosphoserine Aminotransferase Deficiency PHS023
Phosphoserine Phosphatase Deficiency PHS022
Photoallergic Dermatitis PHT004
Photokeratitis PHT002
Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction PHT013
Photoparoxysmal Response 1 PHT010
Photoparoxysmal Response 2 PHT009
Photoparoxysmal Response 3 PHT011
Photosensitive Epilepsy PHT008
Phototoxic Dermatitis PHT003
Phthisical Cornea PHT005
Physical Disorder PHY002
Physical Urticaria PHY008
Physiological Polycythemia PHY001
Pica Disease PCD001
Pick Disease of Brain PCK003
Piebald Trait PBL005
Piebald Trait with Neurologic Defects PBL004
Piepkorn Karp Hickok Syndrome PPK001
Pierpont Syndrome PRP093
Pierre Robin Sequence with Facial and Digital Anomalies PRR030
Pierre Robin Sequence with Pectus Excavatum and Rib and Scapular Anomalies PRR011
Pierre Robin Syndrome PRR016
Pierre Robin Syndrome and Oligodactyly PRR029
Pierre Robin Syndrome Skeletal Dysplasia Polydactyly PRR012
Pierson Syndrome PRS055
Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked PGM029
Pigmentation Defects-Palmoplantar Keratoderma-Skin Carcinoma Syndrome PGM025
Pigmentation Disease PGM003
Pigmented Basal Cell Carcinoma PGM002
Pigmented Nodular Adrenocortical Disease, Primary, 1 PGM021
Pigmented Nodular Adrenocortical Disease, Primary, 2 PGM011
Pigmented Nodular Adrenocortical Disease, Primary, 3 PGM012
Pigmented Nodular Adrenocortical Disease, Primary, 4 PGM022
Pigmented Paravenous Chorioretinal Atrophy PGM007
Pigmented Purpuric Dermatosis PGM028
Pigmented Purpuric Eruption PGM010
Pigmented Villonodular Synovitis PGM001
Pik3ca-Related Overgrowth Spectrum PK3004
Pik3ca-Related Segmental Overgrowth PK3001
Pilar Sheath Acanthoma PLR003
Pilarowski-Bjornsson Syndrome PLR024
Pili Bifurcati PLB003
Pili Gemini PLG007
Pili Torti PLT008
Pili Torti and Developmental Delay PLT021
Pili Torti Developmental Delay Neurological Abnormalities PLT009
Pili Torti Onychodysplasia PLT010
Pili Torti, Early-Onset PLT022
Pillay Syndrome PLL007
Pilo Dento Ungular Dysplasia Microcephaly PLD001
Pilocytic Astrocytoma PLC011
Pilocytic Astrocytoma of Cerebellum PLC004
Pilodental Dysplasia with Refractive Errors PLD002
Pilomatrix Carcinoma PLM177
Pilomatrixoma PLM026
Pilomyxoid Astrocytoma PLM021
Pilonidal Sinus PLN026
Pilotto Syndrome PLT011
Pinched Nerve PNC065
Pineal Cyst PNL021
Pineal Dysgerminoma PNL008
Pineal Gland Astrocytoma PNL001
Pineal Gland Cancer PNL014
Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities PNL019
Pineal Parenchymal Tumor of Intermediate Differenciation PNL022
Pineal Parenchymal Tumor of Intermediate Differentiation PNL002
Pineal Region Choriocarcinoma PNL009
Pineal Region Germinoma PNL011
Pineal Region Immature Teratoma PNL005
Pineal Region Mature Teratoma PNL004
Pineal Region Meningioma PNL003
Pineal Region Teratoma PNL015
Pineal Region Yolk Sac Tumor PNL010
Pineoblastoma PNB001
Pineoblastoma, Childhood PNB003
Pineocytoma PNC056
Pinguecula PNG001
Pinheiro Freire-Maia Miranda Syndrome PNH003
Pink1 Type of Young-Onset Parkinson Disease PNK001
Pinnae Fistula or Cyst PNN004
Pinta Disease PNT003
Pipecolic Acidemia PPC004
Piriformis Syndrome PRF003
Pitt-Hopkins Syndrome PTT014
Pitt-Hopkins-Like Syndrome PTT042
Pitt-Hopkins-Like Syndrome 1 PTT029
Pitt-Hopkins-Like Syndrome 2 PTT030
Pituicytoma PTC005
Pituitary Adenoma PTT006
Pituitary Adenoma 1, Multiple Types PTT056 PITA1
Pituitary Adenoma 2, Growth Hormone-Secreting PTT058
Pituitary Adenoma 3, Multiple Types PTT061
Pituitary Adenoma 4, Acth-Secreting PTT057
Pituitary Adenoma 5, Multiple Types PTT060
Pituitary Adenoma, Prolactin-Secreting PTT048
Pituitary Apoplexy PTT004
Pituitary Carcinoma PTT008
Pituitary Deficiency Due to Empty Sella Turcica Syndrome PTT038
Pituitary Deficiency Due to Rathke's Cleft Cysts PTT062
Pituitary Dermoid and Epidermoid Cysts PTT039
Pituitary Dwarfism with Large Sella Turcica PTT019
Pituitary Gland Disease PTT009
Pituitary Hormone Deficiency, Combined, 1 PTT045
Pituitary Hormone Deficiency, Combined, 2 PTT046
Pituitary Hormone Deficiency, Combined, 3 PTT047
Pituitary Hormone Deficiency, Combined, 4 PTT044
Pituitary Hormone Deficiency, Combined, 6 PTT043
Pituitary Hypoplasia PTT001
Pituitary Infarct PTT010
Pituitary Stalk Interruption Syndrome PTT041
Pituitary Stalk Meningioma PTT005
Pituitary Tumors PTT037
Pituitary-Dependent Cushing's Disease PTT003
Pityriasis Lichenoides PTY004
Pityriasis Lichenoides Chronica PTY005
Pityriasis Lichenoides Et Varioliformis Acuta PTY006
Pityriasis Rosea PTY001
Pityriasis Rotunda PTY007
Pityriasis Rubra Pilaris PTY003
Pityriasis Versicolor PTY002
Piussan Lenaerts Mathieu Syndrome PSS002
Placenta Accreta PLC001
Placenta Disease PLC008
Placenta Praevia PLC009
Placental Abruption PLC007
Placental Choriocarcinoma PLC006
Placental Insufficiency PLC005
Placental Site Trophoblastic Tumor PLC003
Plagiocephaly PLG004
Plague PLG002
Plantar Fascial Fibromatosis PLN003
Plantar Fasciitis PLN007
Plantar Nerve Lesion PLN002
Plantar Verrucous Skin Carcinoma PLN004
Plantar Wart PLN001
Plaque-Form Urticaria Pigmentosa PLQ001
Plasma Cell Leukemia PLS016
Plasma Cell Neoplasm PLS009
Plasma Clot Retraction Factor, Deficiency of PLS033
Plasma Fibronectin Deficiency PLS026
Plasma Protein Metabolism Disease PLS010
Plasma Triglyceride Level Quantitative Trait Locus PLS035
Plasmablastic Lymphoma PLS025
Plasmacytic Leukemia PLS003
Plasmacytoid Variant Infiltrating Bladder Urothelial Carcinoma PLS004
Plasmacytoma PLS011
Plasmalogens Synthesis Deficiency Isolated PLS017
Plasminogen Activator Inhibitor-1 Deficiency PLS029
Plasminogen Deficiency, Type I PLS030
Plasmodium Falciparum Blood Infection Level PLS032
Plasmodium Falciparum Fever Episodes Quantitative Trait Locus 1 PLS034
Plasmodium Falciparum Malaria PLS007
Plasmodium Malariae Malaria PLS008
Plasmodium Ovale Malaria PLS005
Plasmodium Vivax Malaria PLS006
Plastic Bronchitis PLS031
Platelet Abnormalities with Eosinophilia and Immune-Mediated Inflammatory Disease PLT035
Platelet Adenylate Cyclase Activity PLT016
Platelet Aggregation, Spontaneous PLT015
Platelet Disorder, Familial, with Associated Myeloid Malignancy PLT019
Platelet Disorder, Undefined PLT027
Platelet Factor 3 Deficiency PLT028
Platelet Glycoprotein Iv Deficiency PLT004
Platelet Groups--Ko System PLT029
Platelet Groups--Pl System PLT030
Platelet Membrane Fluidity PLT031
Platelet Prostacyclin Receptor Defect PLT034
Platelet Responsiveness to Adrenaline, Depressed PLT032
Platelet Signal Processing Defect PLT033
Platelet-Activating Factor Acetylhydrolase Deficiency PLT006
Platyspondylic Lethal Skeletal Dysplasia, Torrance Type PLT026
Pleoconial Myopathy with Salt Craving PLC012
Pleomorphic Adenoma PLM014
Pleomorphic Adenoma Carcinoma PLM009
Pleomorphic Carcinoma PLM016
Pleomorphic Lipoma PLM005
Pleomorphic Liposarcoma PLM019
Pleomorphic Rhabdomyosarcoma PLM030
Pleomorphic Xanthoastrocytoma PLM020
Plethora of Newborn PLT001
Pleural Cancer PLR006
Pleural Disease PLR022
Pleural Empyema PLR007
Pleural Lipoma PLR002
Pleural Tuberculosis PLR001
Pleurisy PLR008
Pleuro-Pericardial Cyst PLR014
Pleuroparenchymal Fibroelastosis PLR025
Pleuropneumonia PLR005
Pleuropulmonary Blastoma PLR004
Pleuropulmonary Blastoma Type 1 PLR018
Pleuropulmonary Blastoma Type 2 PLR019
Pleuropulmonary Blastoma Type 3 PLR020
Plexiform Neurofibroma PLX002
Plexiform Schwannoma PLX001
Plexopathy PLX004
Plexosarcoma PLX003
Plica Syndrome PLC002
Plod1-Related Kyphoscoliotic Ehlers-Danlos Syndrome PLD003
Plp1-Related Disorders PLP005
Plum Allergy PLM144
Plummer Vinson Syndrome PLM049
Plummer's Disease PLM011
Pmm2-Congenital Disorder of Glycosylation PMM002
Pmp2-Related Charcot-Marie-Tooth Disease Type 1 PMP012
Pneumatosis Cystoides Intestinalis PNM003
Pneumococcal Meningitis PNM013
Pneumoconiosis PNM006
Pneumoconiosis Due to Talc PNM004
Pneumocystic Carinii Pneumonia PNM009
Pneumocystosis PNM001
Pneumonia PNM007
Pneumonia Caused by Pseudomonas Aeruginosa Infection PNM022
Pneumonic Plague PNM005
Pneumonic Tularemia PNM002
Pneumothorax PNM008
Pneumothorax, Primary Spontaneous PNM010
Pnpla6-Related Disorders PNP004
Podder-Tolmie Syndrome PDD001
Podoconiosis PDC001
Poems Syndrome PMS001
Poikiloderma with Neutropenia PKL001
Poikiloderma, Hereditary Fibrosing, with Tendon Contractures, Myopathy, and Pulmonary Fibrosis PKL002
Poikiloderma, Hereditary Sclerosing PKL003
Pointer Syndrome PNT008
Pol Iii-Related Leukodystrophies PLR009
Poland Syndrome PLN006
Polg-Related Disorders PLG003
Poliomyelitis PLM031
Poliomyelitis in Patients with Immunodeficiencies Deemed at Risk PLM110
Pollen Allergy PLL012
Polr3-Related Leukodystrophy PLR023
Polyarteritis Nodosa PLY017
Polyarteritis Nodosa, Childhood-Onset PLY112
Polyarticular Onset Juvenile Idiopathic Arthritis PLY065
Polyclonal Hypergammaglobulinemia PLY010
Polyclonal Hyperviscosity Syndrome PLY128
Polycystic Bone Disease PLY028
Polycystic Echinococcosis PLY003
Polycystic Kidney Disease PLY014
Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease PLY168
Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease PLY172
Polycystic Kidney Disease 3 with or Without Polycystic Liver Disease PLY171
Polycystic Kidney Disease 4 PLY176
Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease PLY170
Polycystic Kidney Disease 5 PLY141
Polycystic Kidney Disease, Infantile Severe, with Tuberous Sclerosis PLY116
Polycystic Kidney, Cataract, and Congenital Blindness PLY155
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy PLY082
Polycystic Liver Disease PLY023
Polycystic Liver Disease 1 with or Without Kidney Cysts PLY169
Polycystic Liver Disease 2 with or Without Kidney Cysts PLY173
Polycystic Liver Disease 3 with or Without Kidney Cysts PLY174
Polycystic Liver Disease 4 with or Without Kidney Cysts PLY175
Polycystic Ovary Syndrome PLY011
Polycystic Ovary Syndrome 1 PLY105
Polycythemia PLY018
Polycythemia Due to Hypoxia PLY005
Polycythemia Vera PLY001
Polydactyly PLY006
Polydactyly Cleft Lip Palate Psychomotor Retardation PLY030
Polydactyly Syndrome Middle Ray Duplication PLY035
Polydactyly, Postaxial, Type A1 PLY147
Polydactyly, Postaxial, Type A2 PLY163
Polydactyly, Postaxial, Type A3 PLY053
Polydactyly, Postaxial, Type A4 PLY054
Polydactyly, Postaxial, Type A5 PLY103
Polydactyly, Postaxial, Type A6 PLY101
Polydactyly, Postaxial, Type A7 PLY144
Polydactyly, Postaxial, with Dental and Vertebral Anomalies PLY134
Polydactyly, Postaxial, with Progressive Myopia PLY135
Polydactyly, Preaxial I PLY136
Polydactyly, Preaxial Ii PLY148
Polydactyly, Preaxial Iii PLY137
Polydactyly, Preaxial Iv PLY149
Polyembryoma PLY036
Polyembryoma of the Ovary PLY009
Polyendocrine-Polyneuropathy Syndrome PLY115
Polyglucosan Body Myopathy 1 with or Without Immunodeficiency PLY118
Polyglucosan Body Myopathy 2 PLY114
Polyglucosan Body Neuropathy, Adult Form PLY158
Polyhydramnios PLY012
Polyhydramnios, Chronic Idiopathic PLY160
Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy PLY062
Polykaryocytosis Inducer PLY150
Polymerase Proofreading-Related Adenomatous Polyposis PLY138
Polymicrogyria PLY024
Polymicrogyria Turricephaly Hypogenitalism PLY037
Polymicrogyria, Bilateral Frontoparietal PLY117
Polymicrogyria, Bilateral Perisylvian, Autosomal Recessive PLY167
Polymicrogyria, Bilateral Perisylvian, X-Linked PLY161
Polymicrogyria, Bilateral Temporooccipital PLY110
Polymicrogyria, Perisylvian, with Cerebellar Hypoplasia and Arthrogryposis PLY126
Polymorphic Reticulosis PLY039
Polymorphous Low-Grade Adenocarcinoma PLY040
Polymyoclonus, Infantile PLY157
Polymyositis PLY041
Polyneuropathy PLY019
Polyneuropathy Associated with Igm Monoclonal Gammapathy with Anti-Mag PLY113
Polyneuropathy Due to Drug PLY008
Polyneuropathy in Collagen Vascular Disease PLY002
Polyneuropathy-Intellectual Disability-Acromicria-Premature Menopause Syndrome PLY127
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract PLY052
Polyneuropathy, Lethal Neonatal, Axonal Sensorimotor, Autosomal Recessive PLY164
Polyomavirus Allograft Nephropathy PLY043
Polyosteolysis-Hyperostosis Syndrome PLY165
Polyp of Corpus Uteri PLY004
Polyp of Middle Ear PLY016
Polyposis of Gastric Fundus Without Polyposis Coli PLY153
Polyposis Syndrome, Hereditary Mixed, 1 PLY162
Polyposis Syndrome, Hereditary Mixed, 2 PLY066
Polyposis, Gastric PLY073
Polyposis, Intestinal, Scattered and Discrete PLY151
Polyposis, Intestinal, with Multiple Exostoses PLY152
Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes PLY131
Polyps, Multiple and Recurrent Inflammatory Fibroid, Gastrointestinal PLY154
Polyradiculoneuropathy PLY020
Polyradiculoneuropathy Associated with Igg/iga/igm Monoclonal Gammopathy Without Known Antibodies PLY087
Polyradiculopathy PLY021
Polyrrhinia PLY086
Polysaccharide, Storage of Unusual PLY159
Polysubstance Abuse PLY068
Polysyndactyly Trigonocephaly Agenesis of Corpus Callosum PLY047
Polysyndactyly with Cardiac Malformation PLY133
Polysyndactyly, Crossed PLY132
Polyunsaturated Fatty Acids Plasma Level Quantitative Trait Locus 1 PLY166
Polyvalvular Heart Disease Syndrome PLY088
Polyvesicular Vitelline Pattern Ovarian Yolk Sac Tumor PLY007
Polyvesicular Vitelline Pattern Testicular Yolk Sac Tumor PLY015
Pompholyx PMP010
Poncet-Spiegler's Cylindroma PNC057
Pontiac Fever PNT001
Pontine Autosomal Dominant Microangiopathy with Leukoencephalopathy PNT040
Pontine Hemorrhage PNT023
Pontine Tegmental Cap Dysplasia PNT009
Pontocerebellar Hypoplasia PNT019
Pontocerebellar Hypoplasia Type 1 PNT010
Pontocerebellar Hypoplasia, Type 10 PNT033
Pontocerebellar Hypoplasia, Type 11 PNT050
Pontocerebellar Hypoplasia, Type 1a PNT045
Pontocerebellar Hypoplasia, Type 1b PNT018
Pontocerebellar Hypoplasia, Type 1c PNT035
Pontocerebellar Hypoplasia, Type 2a PNT044
Pontocerebellar Hypoplasia, Type 2b PNT047
Pontocerebellar Hypoplasia, Type 2c PNT048
Pontocerebellar Hypoplasia, Type 2d PNT049
Pontocerebellar Hypoplasia, Type 2e PNT034
Pontocerebellar Hypoplasia, Type 2f PNT042
Pontocerebellar Hypoplasia, Type 3 PNT037
Pontocerebellar Hypoplasia, Type 4 PNT043
Pontocerebellar Hypoplasia, Type 5 PNT046
Pontocerebellar Hypoplasia, Type 6 PNT036
Pontocerebellar Hypoplasia, Type 7 PNT039
Pontocerebellar Hypoplasia, Type 8 PNT030
Pontocerebellar Hypoplasia, Type 9 PNT032
Pontoneocerebellar Hypoplasia PNT016
Poorly Differentiated Thymic Neuroendocrine Carcinoma PRL043
Popliteal Cyst PPL054
Popliteal Pterygium Syndrome PPL025 PPS
Popliteal Pterygium Syndrome, Lethal Type PPL059
Porencephaly PRN026
Porencephaly 1 PRN053
Porencephaly 2 PRN047
Porencephaly, Cerebellar Hypoplasia, and Internal Malformations PRN057
Poretti-Boltshauser Syndrome PRT101
Porokeratosis PRK001
Porokeratosis 1, Multiple Types PRK082
Porokeratosis 2, Palmar, Plantar, and Disseminated Type PRK076
Porokeratosis 3, Multiple Types PRK080
Porokeratosis 4, Disseminated Superficial Actinic Type PRK095
Porokeratosis 5, Disseminated Superficial Actinic Type PRK097
Porokeratosis 6, Multiple Types PRK084
Porokeratosis 7, Multiple Types PRK075
Porokeratosis 8, Disseminated Superficial Actinic Type PRK067
Porokeratosis 9, Multiple Types PRK074
Porokeratotic Eccrine Ostial and Dermal Duct Nevus PRK047
Porphyria PRP029
Porphyria Cutanea Tarda PRP003
Porphyria Cutanea Tarda, Type I PRP091
Porphyria Variegata PRP032
Porphyria, Acute Hepatic PRP056
Porphyria, Acute Intermittent PRP083
Porphyria, Congenital Erythropoietic PRP082
Portal Hypertension PRT013
Portal Hypertension Due to Infrahepatic Block PRT053
Portal Hypertension, Noncirrhotic PRT112
Portal Vein Thrombosis PRT018
Portal Vein, Cavernous Transformation of PRT124
Positive Rheumatoid Factor Polyarthritis PST038
Posner-Schlossman Syndrome PSN006
Post-Infectious Myocarditis PST043
Post-Streptococcal Neurologic Disorders PST045
Post-Surgical Hypoinsulinemia PST024
Post-Thrombotic Syndrome PST095
Post-Transplant Lymphoproliferative Disease PST046
Post-Traumatic Epilepsy PST047
Post-Traumatic Stress Disorder PST028
Post-Vaccinal Encephalitis PST007
Postauricular Lymphadenitis PST006
Postaxial Acrofacial Dysostosis PST049
Postaxial Oligodactyly, Tetramelic PST104
Postcardiotomy Right Ventricular Failure PST076
Postcholecystectomy Syndrome PST030
Postcricoid Region Cancer PST031
Postencephalitic Parkinson Disease PST027
Posterior Cerebral Artery Infarction PST018
Posterior Column Ataxia PST040
Posterior Column Ataxia with Retinitis Pigmentosa PST036
Posterior Corneal Pigmentation PST012
Posterior Cortical Atrophy PST086
Posterior Dislocation of Lens PST025
Posterior Foramen Magnum Meningioma PST023
Posterior Hypospadias PST093
Posterior Mediastinum Cancer PST013
Posterior Meningocele PST077
Posterior Myocardial Infarction PST001
Posterior Pituitary Gland Neoplasm PST034
Posterior Polar Cataract PST016
Posterior Scleritis PST008
Posterior Urethra Cancer PST032
Posterior Urethral Valves PST041
Posterior Uveal Melanoma PST022
Posterior Uveitis PST005
Posterior Valve Urethra PST042
Posteroinferior Myocardial Infarction PST002
Posterolateral Myocardial Infarction PST017
Postgastrectomy Syndrome PST035
Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma PST004
Postherpetic Neuralgia PST053
Postinfectious Encephalomyelitis PST054
Postinfectious Vasculitis PST098
Postinflammatory Pulmonary Fibrosis PST015
Postlingual Non-Syndromic Genetic Deafness PST097
Postmenopausal Atrophic Vaginitis PST029
Postorgasmic Illness Syndrome PST044
Postpartum Depression PST021
Postpartum Psychosis PST103
Postpoliomyelitis Syndrome PST020
Postsurgical Hypothyroidism PST014
Postsynaptic Congenital Myasthenic Syndromes PST063
Posttransplant Acute Limbic Encephalitis PST092
Postural Hypotension PST055
Postural Orthostatic Tachycardia Syndrome PST048
Potocki-Lupski Syndrome PTC002
Potocki-Shaffer Syndrome PTC001
Potter's Syndrome PTT002
Pouchitis PCH007
Powassan Encephalitis PWS001
Ppoma PPM002
Ppp2r5d-Related Intellectual Disability PPP001
Pr Interval, Variation in PRN062
Prader-Willi Habitus, Osteopenia, and Camptodactyly PRD014
Prader-Willi Syndrome PRD006
Prader-Willi Syndrome Due to Imprinting Mutation PRD025
Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15 PRD028
Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion PRD027
Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 PRD022
Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 PRD023
Prader-Willi Syndrome Due to Translocation PRD024
Prader-Willi-Like Syndrome Due to a Point Mutation PRD042
Pre-Descemet Corneal Dystrophy PRD026
Pre-Eclampsia PRC016
Pre-Malignant Neoplasm PRM023
Preauricular Fistulae, Congenital PRR015 PAFC
Preauricular Sinus PRR018
Preauricular Tag, Isolated, Autosomal Dominant, 1 PRR023
Preaxial Deficiency, Postaxial Polydactyly, and Hypospadias PRX093
Preaxial Hallucal Polydactyly PRX085
Preaxial Polydactyly of Fingers PRX078
Preaxial Polydactyly-Colobomata-Intellectual Disability Syndrome PRX083
Precocious Epileptic Encephalopathy PRC023
Precocious Myoclonic Encephalopathy PRC024
Precocious Puberty PRC019
Precocious Puberty, Central, 1 PRC047
Precocious Puberty, Central, 2 PRC046
Precocious Puberty, Gonadotropin-Dependent PRC025
Precocious Puberty, Male-Limited PRC038
Precursor B Lymphoblastic Lymphoma/leukemia PRC004
Precursor Lymphoblastic Lymphoma/leukemia PRC017
Precursor T-Cell Acute Lymphoblastic Leukemia PRC049
Precursor T-Lymphoblastic Lymphoma/leukemia PRC018
Precursor T-Lymphoblastic Lymphoma/leukemia Refractory PRC009
Prediabetes Syndrome PRD004
Predominantly Cortical Thymoma PRD001
Preeclampsia/eclampsia 1 PRC031
Preeclampsia/eclampsia 2 PRC032
Preeclampsia/eclampsia 3 PRC033
Preeclampsia/eclampsia 4 PRC034
Preeclampsia/eclampsia 5 PRC045
Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma PRG005
Pregnancy Adenoma PRG010
Pregnancy Loss, Recurrent 1 PRG092
Pregnancy Loss, Recurrent 2 PRG096
Pregnancy Loss, Recurrent 3 PRG093
Preimplantation Embryonic Lethality 1 PRM252
Preimplantation Embryonic Lethality 2 PRM251
Prekallikrein Deficiency PRK005
Prekallikrein Deficiency, Congenital PRK014
Prelingual Non-Syndromic Genetic Deafness PRL044
Premature Aging Syndrome, Okamoto Type PRM291
Premature Aging Syndrome, Penttinen Type PRM206
Premature Centromere Division PRM290
Premature Chromatid Separation Trait PRM087
Premature Closure of the Arterial Duct PRM160
Premature Ejaculation PRM003
Premature Menopause PRM013
Premature Ovarian Failure 1 PRM196
Premature Ovarian Failure 10 PRM207
Premature Ovarian Failure 11 PRM254
Premature Ovarian Failure 12 PRM255
Premature Ovarian Failure 13 PRM253
Premature Ovarian Failure 14 PRM292
Premature Ovarian Failure 2a PRM176
Premature Ovarian Failure 2b PRM091
Premature Ovarian Failure 3 PRM089
Premature Ovarian Failure 5 PRM094
Premature Ovarian Failure 6 PRM090
Premature Ovarian Failure 7 PRM093
Premature Ovarian Failure 8 PRM192
Premature Ovarian Failure 9 PRM191
Premenstrual Tension PRM020
Prenatal Benign Hypophosphatasia PRN048
Prenatal Bowing PRN066
Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures PRN061
Prepapillary Vascular Loops PRP097
Prepuce Cancer PRP010
Preretinal Fibrosis PRR004
Presbyopia PRS025
Presenile Dementia, Kraepelin Type PRS056
Presynaptic Congenital Myasthenic Syndromes PRS124
Preterm Premature Rupture of the Membranes PRT082
Priapism PRP007
Priapism, Familial Idiopathic PRP095
Prickle1-Related Progressive Myoclonus Epilepsy with Ataxia PRC020
Prieto X-Linked Mental Retardation Syndrome PRT055
Primary Adult Heart Tumor PRM287
Primary Agammaglobulinemia PRM038
Primary Aldosteronism, Seizures, and Neurologic Abnormalities PRM183
Primary Amebic Meningoencephalitis PRM004
Primary Anetoderma PRM145
Primary Angiitis of the Central Nervous System PRM039
Primary Angle-Closure Glaucoma PRM024
Primary Autosomal Recessive Microcephalies and Seckel Syndrome Spectrum Disorders PRM174
Primary Bacterial Infectious Disease PRM025
Primary Biliary Cholangitis PRM236
Primary Biliary Cirrhosis PRM006
Primary Bone Cancer PRM243
Primary Bone Lymphoma PRM151
Primary Central Nervous System Lymphoma PRM226
Primary Cerebellar Degeneration PRM015
Primary Ciliary Dyskinesia PRM011
Primary Condylar Hyperplasia PRM249
Primary Congenital Glaucoma PRM032
Primary Cutaneous Aggressive Epidermotropic Cd8+ T-Cell Lymphoma PRM131
Primary Cutaneous Amyloidosis PRM001
Primary Cutaneous Anaplastic Large Cell Lymphoma PRM155
Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma PRM132
Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type PRM127
Primary Cutaneous Follicle Center Lymphoma PRM128
Primary Cutaneous Gamma/delta-Positive T-Cell Lymphoma PRM130
Primary Cutaneous Marginal Zone B-Cell Lymphoma PRM129
Primary Cutaneous Peripheral T-Cell Lymphoma Not Otherwise Specified PRM250
Primary Cutaneous Plasmacytosis PRM233
Primary Effusion Lymphoma PRM042
Primary Essential Cutis Verticis Gyrata PRM185
Primary Eye Hypotony PRM009
Primary Familial Brain Calcification PRM175
Primary Fanconi Syndrome PRM200
Primary Hepatic Neuroendocrine Carcinoma PRM205
Primary Hypereosinophilic Syndrome PRM149
Primary Hyperoxaluria PRM002
Primary Hyperparathyroidism PRM005
Primary Hypertrophic Osteoarthropathy PRM018
Primary Hypomagnesemia PRM237
Primary Immunodeficiency with Post-Measles-Mumps-Rubella Vaccine Viral Infection PRM247
Primary Intestinal Lymphangiectasia PRM158
Primary Intrahepatic Lithiasis PRM248
Primary Intralymphatic Angioendothelioma PRM238
Primary Lacrimal Atrophy PRM007
Primary Laryngeal Lymphangioma PRM134
Primary Lateral Sclerosis, Adult, 1 PRM092
Primary Lateral Sclerosis, Juvenile PRM195
Primary Localized Amyloidosis PRM150
Primary Lymphoma of the Conjunctiva PRM148
Primary Malignant Melanoma of the Cervix PRM047
Primary Malignant Melanoma of the Conjunctiva PRM048
Primary Mediastinal B-Cell Lymphoma PRM293
Primary Mediastinal Large B-Cell Lymphoma PRM163
Primary Megaureter, Adult-Onset Form PRM147
Primary Melanoma of the Central Nervous System PRM139
Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome PRM187
Primary Non-Gestational Choriocarcinoma of Ovary PRM193
Primary Oculocerebral Lymphoma PRM142
Primary Optic Atrophy PRM016
Primary Orthostatic Hypotension PRM227
Primary Orthostatic Tremor PRM050
Primary Pediatric Heart Tumor PRM286
Primary Peritoneal Carcinoma PRM126
Primary Peritoneal Serous/papillary Carcinoma PRM194
Primary Pigmented Nodular Adrenocortical Disease PRM051
Primary Plasmacytoma of the Bone PRM165
Primary Polyarteritis Nodosa PRM222
Primary Polycythemia PRM012
Primary Progressive Apraxia of Speech PRM153
Primary Progressive Freezing Gait PRM157
Primary Progressive Multiple Sclerosis PRM108
Primary Pulmonary Lymphoma PRM133
Primary Release Disorder of Platelets PRM053
Primary Sjögren Syndrome PRM294
Primary Syphilis PRM022
Primary Syringomyelia PRM168
Primary Systemic Mycosis PRM026
Primary Tethered Cord Syndrome PRM246
Primary Thrombocytopenia PRM225
Primary Trimethylaminuria PRM209
Primary Tubular Proximal Acidosis PRM055
Primary Unilateral Adrenal Hyperplasia PRM146
Primitive Neuroectodermal Tumor of the Cervix Uteri PRM284
Primitive Neuroectodermal Tumor of the Corpus Uteri PRM283
Primitive Portal Vein Thrombosis PRM285
Primrose Syndrome PRM056
Prion Disease PRN023
Prkar1b-Related Neurodegenerative Dementia with Intermediate Filaments PRK068
Proboscis Lateralis PRB002
Proctitis PRC003
Progeria Variant Syndrome Ruvalcaba Type PRG022
Progeria-Associated Arthropathy PRG089
Progeroid Facial Appearance with Hand Anomalies PRG132
Progeroid Short Stature with Pigmented Nevi PRG023
Progeroid Syndrome Petty Type PRG024
Progeroid Syndrome, Neonatal PRG123
Progeroid Syndrome, Penttinen Type PRG025
Progesterone Resistance PRG014
Progesterone-Receptor Negative Breast Cancer PRG003
Progesterone-Receptor Positive Breast Cancer PRG002
Prognathism, Mandibular PRG122
Progressive Black Carbon Hyperpigmentation of Infancy PRG027
Progressive Bulbar Palsy PRG007
Progressive Cavitating Leukoencephalopathy PRG076
Progressive Encephalomyelitis with Rigidity and Myoclonus PRG110
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 PRG130
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 PRG038
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 PRG039
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 PRG040
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 5 PRG041
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 6 PRG103
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1 PRG131
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 2 PRG102
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 3 PRG129
Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 4 PRG128
Progressive Familial Heart Block PRG126
Progressive Familial Heart Block, Type Ia PRG042 PFHB1A
Progressive Familial Heart Block, Type Ib PRG043
Progressive Familial Heart Block, Type Ii PRG101
Progressive Kinking of the Hair, Acquired PRG032
Progressive Locomotor Ataxia PRG048
Progressive Multifocal Leukoencephalopathy PRG009
Progressive Muscular Atrophy PRG001
Progressive Myoclonic Epilepsy Type 5 PRG133
Progressive Myoclonus Epilepsy PRG011
Progressive Myoclonus Epilepsy, Lafora Type PRG074
Progressive Nodular Histiocytosis PRG077
Progressive Non-Fluent Aphasia PRG033
Progressive Non-Infectious Anterior Vertebral Fusion PRG080
Progressive Peripheral Pterygium PRG012
Progressive Relapsing Multiple Sclerosis PRG090
Progressive Supranuclear Palsy-Corticobasal Syndrome PRG116
Progressive Supranuclear Palsy-Progressive Non-Fluent Aphasia Syndrome PRG115
Progressive Supranuclear Palsy-Pure Akinesia with Gait Freezing Syndrome PRG117
Progressive Transformation of Germinal Centers PRG036
Prolactin Deficiency with Obesity and Enlarged Testes PRL046
Prolactin Deficiency, Isolated PRL037
Prolactin Producing Pituitary Tumor PRL010
Prolapse of Female Genital Organ PRL015
Prolapse of Lacrimal Gland PRL002
Prolapse of Urethra PRL004
Prolidase Deficiency PRL019
Proliferating Trichilemmal Cyst PRL042
Proliferative Fasciitis PRL005
Proliferative Glomerulonephritis PRL003
Proliferative Type Fibrocystic Change of Breast PRL016
Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome PRL023
Proliferative Verrucous Leukoplakia PRL048
Proline-Negative Auxotroph of Hamster, Complementation of PRL045
Prolonged Electroretinal Response Suppression PRL047
Prolymphocytic Leukemia PRL017
Pronation-Supination of the Forearm, Impairment of PRN064
Prop1-Related Combined Pituitary Hormone Deficiency PRP035
Properdin Deficiency PRP033
Properdin Deficiency, X-Linked PRP038
Propionic Acidemia PRP001
Propriospinal Myoclonus PRP068
Proprotein Convertase 1/3 Deficiency PRP098
Propylthiouracil Embryofetopathy PRP094
Prosencephaly Cerebellar Dysgenesis PRS057
Prosopagnosia PRS013
Prosopagnosia, Hereditary PRS058
Prostaglandin-Endoperoxide Synthase Deficiency PRS059
Prostate Adenoid Cystic Carcinoma PRS019
Prostate Angiosarcoma PRS005
Prostate Calculus PRS007
Prostate Cancer PRS040
Prostate Cancer Aggressiveness Quantitative Trait Locus on Chromosome 19 PRS133
Prostate Cancer, Hereditary, 1 PRS097
Prostate Cancer, Hereditary, 10 PRS074
Prostate Cancer, Hereditary, 11 PRS117
Prostate Cancer, Hereditary, 12 PRS070
Prostate Cancer, Hereditary, 13 PRS071
Prostate Cancer, Hereditary, 14 PRS075
Prostate Cancer, Hereditary, 15 PRS076
Prostate Cancer, Hereditary, 2 PRS114
Prostate Cancer, Hereditary, 3 PRS134
Prostate Cancer, Hereditary, 4 PRS135
Prostate Cancer, Hereditary, 5 PRS079
Prostate Cancer, Hereditary, 6 PRS136
Prostate Cancer, Hereditary, 7 PRS080
Prostate Cancer, Hereditary, 8 PRS130
Prostate Cancer, Hereditary, 9 PRS081
Prostate Cancer, Hereditary, X-Linked 1 PRS083
Prostate Cancer, Hereditary, X-Linked 2 PRS084
Prostate Cancer, Progression and Metastasis of PRS069
Prostate Cancer/brain Cancer Susceptibility PRS131
Prostate Carcinoma in Situ PRS031
Prostate Colloid Adenocarcinoma PRS001
Prostate Disease PRS042
Prostate Embryonal Rhabdomyosarcoma PRS010
Prostate Leiomyoma PRS022
Prostate Leiomyosarcoma PRS032
Prostate Lymphoma PRS002
Prostate Malignant Phyllodes Tumor PRS003
Prostate Neuroendocrine Neoplasm PRS017
Prostate Rhabdomyosarcoma PRS043
Prostate Sarcoma PRS044
Prostate Signet Ring Cell Adenocarcinoma PRS015
Prostate Small Cell Carcinoma PRS008
Prostate Squamous Cell Carcinoma PRS004
Prostate Stromal Sarcoma PRS009
Prostate Transitional Cell Carcinoma PRS027
Prostatic Acinar Adenocarcinoma PRS006
Prostatic Adenoma PRS021
Prostatic Cyst PRS014
Prostatic Hyperplasia, Benign PRS129
Prostatic Hypertrophy PRS045
Prostatic Malacoplakia Associated with Prostatic Abscess PRS060
Prostatic Stromal Proliferation of Uncertain Malignant Potential PRS061
Prostatic Urethra Urothelial Carcinoma PRS028
Prostatic Urethral Cancer PRS046
Prostatitis PRS047
Prostatocystitis PRS020
Prosthetic Joint Infection PRS115
Protein C Deficiency PRT011
Protein R Deficiency PRT056
Protein S Acquired Deficiency PRT104
Protein S Deficiency PRT014
Protein Z Deficiency PRT130
Protein-Deficiency Anemia PRT025
Protein-Energy Malnutrition PRT038
Protein-Losing Enteropathy PRT019
Proteinuria, Low Molecular Weight, with Hypercalciuria and Nephrocalcinosis PRT121
Proteolytic Capacity of Plasma PRT117
Proteus Like Syndrome Mental Retardation Eye Defect PRT057
Proteus Syndrome PRT008
Proteus-Like Syndrome PRT063
Prothrombin Deficiency PRT012
Prothrombin Deficiency, Congenital PRT129
Prothrombin-Related Thrombophilia PRT045
Protocadherin 3 PRT123
Proton-Pump Inhibitor-Responsive Esophageal Eosinophilia PRT107
Protoplasmic Astrocytoma PRT005
Protoporphyria, Erythropoietic PRT118
Protoporphyria, Erythropoietic, X-Linked PRT094
Protozoal Dysentery PRT022
Protrusio Acetabuli PRT119
Proximal Chromosome 18q Deletion Syndrome PRX013
Proximal Myopathy with Focal Depletion of Mitochondria PRX095
Proximal Spinal Muscular Atrophy PRX014
Proximal Symphalangism PRX021
Prp Systemic Amyloidosis PRP089
Prrt2-Associated Paroxysmal Movement Disorders PRR035
Prss1-Related Hereditary Pancreatitis PRS050
Prune Belly Syndrome PRN038 PBS
Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness PRN067
Prurigo Nodularis PRR013
Pruritic Urticarial Papules and Plaques of Pregnancy PRR031
Pruritus, Hereditary Localized PRR034
Psammomatous Meningioma PSM001
Pseudo Pelger-Huet Anomaly PSD024
Pseudo-Gaucher Disease PSD023
Pseudo-Meigs Syndrome PSD084
Pseudo-Torch Syndrome 1 PSD106
Pseudo-Torch Syndrome 2 PSD107
Pseudo-Turner Syndrome PSD047
Pseudo-Von Willebrand Disease PSD048
Pseudoachondroplasia PSD012
Pseudoachondroplastic Dysplasia 2 PSD025
Pseudoacromegaly with Severe Insulin Resistance PSD116
Pseudoainhum PSD026
Pseudoangiomatous Stromal Hyperplasia PSD079
Pseudoarthrogryposis PSD109
Pseudoarthrosis PSD086
Pseudoarylsulfatase a Deficiency PSD028
Pseudoatrophoderma Colli PSD110
Pseudobulbar Affect PSD088
Pseudobulbar Palsy PSD001
Pseudocholinesterase, Increase in Plasma Level of PSD111
Pseudodiastrophic Dysplasia PSD030
Pseudofolliculitis Barbae PSD078
Pseudoglandular Variant Testicular Seminoma PSD013
Pseudohermaphrodism Anorectal Anomalies PSD031
Pseudohermaphroditism PSD009
Pseudohermaphroditism, Female, with Skeletal Anomalies PSD102
Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak PSD063
Pseudohypoaldosteronism PSD003
Pseudohypoaldosteronism, Type I, Autosomal Dominant PSD112
Pseudohypoaldosteronism, Type I, Autosomal Recessive PSD114
Pseudohypoaldosteronism, Type Iia PSD090
Pseudohypoaldosteronism, Type Iib PSD094
Pseudohypoaldosteronism, Type Iic PSD068
Pseudohypoaldosteronism, Type Iid PSD093
Pseudohypoaldosteronism, Type Iie PSD092
Pseudohypoparathyroidism PSD015
Pseudohypoparathyroidism, Type Ia PSD108 PHP1A
Pseudohypoparathyroidism, Type Ib PSD066
Pseudohypoparathyroidism, Type Ic PSD117
Pseudohypoparathyroidism, Type Ii PSD104
Pseudoinflammatory Fundus Dystrophy PSD036
Pseudomarfanism PSD037
Pseudomembranous Conjunctivitis PSD004
Pseudomonas Stutzeri Infections PSD038
Pseudomongolism PSD039
Pseudomonilethrix PSD113
Pseudomyotonia PSD040
Pseudomyxoma Peritonei PSD007
Pseudopapilledema PSD008
Pseudopapilledema Blepharophimosis Hand Anomalies PSD042
Pseudopapilledema, Ocular Hypotelorism, Blepharophimosis, and Hand Anomalies PSD103
Pseudopelade of Brocq PSD043
Pseudopili Annulati PSD118
Pseudopolycythaemia PSD044
Pseudopseudohypoparathyroidism PSD014
Pseudopterygium PSD006
Pseudoretinitis Pigmentosa PSD005
Pseudosarcomatous Fibromatosis PSD016
Pseudotrisomy 13 Syndrome PSD046
Pseudotyphus of California PSD085
Pseudounicornuate Uterus PSD091
Pseudouridinuria and Mental Defect PSD115
Pseudovaginal Perineoscrotal Hypospadias PSD021
Pseudovascular Skin Squamous Cell Carcinoma PSD011
Pseudoxanthoma Elasticum PSD087
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency PSD059
Pseudoxanthoma Elasticum-Like Papillary Dermal Elastolysis PSD105
Pseudoxanthoma Elasticum-Like Skin Manifestations with Retinitis Pigmentosa PSD101
Pseudoxanthoma Elasticum, Forme Fruste PSD050
Pseudoxanthomatous Diffuse Cutaneous Mastocytosis PSD083
Psoriasis PSR002
Psoriasis 1 PSR023
Psoriasis 10 PSR031
Psoriasis 11 PSR032
Psoriasis 12 PSR033
Psoriasis 13 PSR018
Psoriasis 14, Pustular PSR021
Psoriasis 15, Pustular PSR022
Psoriasis 2 PSR017
Psoriasis 3 PSR024
Psoriasis 4 PSR025
Psoriasis 5 PSR026
Psoriasis 6 PSR027
Psoriasis 7 PSR028
Psoriasis 8 PSR030
Psoriasis 9 PSR029
Psoriatic Arthritis PSR001
Psoriatic Juvenile Idiopathic Arthritis PSR016
Psychogenic Movement PSY012
Psychologic Dyspareunia PSY002
Psychologic Vaginismus PSY001
Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism PSY014
Psychosexual Disorder PSY003
Psychosocial Short Stature PSY015
Psychotic Disorder PSY004
Pten Hamartoma Tumor Syndrome PTN006
Pterigium Colli PTR007
Pterygia, Mental Retardation, and Distinctive Craniofacial Features PTR028
Pterygium Colli and Mental Retardation with Facial and Digital Anomalies PTR031
Pterygium Colli Mental Retardation Digital Anomalies PTR009
Pterygium Colli, Isolated PTR033
Pterygium of Conjunctiva and Cornea PTR030
Pterygium, Antecubital PTR029
Pthirus Pubis Infestation PTH001
Ptosis PTS002
Ptosis Strabismus Diastasis PTS006
Ptosis-Syndactyly-Learning Difficulties Syndrome PTS016
Ptosis-Upper Ocular Movement Limitation-Absence of Lacrimal Punctum Syndrome PTS015
Ptosis, Hereditary Congenital 1 PTS018
Ptosis, Hereditary Congenital 2 PTS010
Ptosis, Strabismus, and Ectopic Pupils PTS017
Pubic Bone Dysplasia PBC001
Pudendal Neuralgia PDN001
Puerperal Pulmonary Embolism PRP011
Puerto Rican Infant Hypotonia Syndrome PRT108
Pulmonary Alveolar Microlithiasis PLM017
Pulmonary Alveolar Proteinosis PLM006
Pulmonary Alveolar Proteinosis, Acquired PLM150
Pulmonary Arterio-Veinous Fistula PLM051
Pulmonary Arteriovenous Fistulas PLM151
Pulmonary Arteriovenous Malformation PLM052
Pulmonary Artery Agenesis PLM053
Pulmonary Artery Choriocarcinoma PLM023
Pulmonary Artery Coming from Patent Ductus Arteriosus PLM119
Pulmonary Artery Coming from the Aorta PLM054
Pulmonary Artery Familial Dilatation PLM055
Pulmonary Artery Hypoplasia PLM116
Pulmonary Artery Leiomyosarcoma PLM004
Pulmonary Aspergilloma PLM007
Pulmonary Atresia with Intact Ventricular Septum PLM058
Pulmonary Atresia with Ventricular Septal Defect PLM059
Pulmonary Blastoma PLM032
Pulmonary Branches Stenosis PLM060
Pulmonary Bullae Causing Pneumothorax PLM168
Pulmonary Coin Lesion PLM028
Pulmonary Disease, Chronic Obstructive PLM129
Pulmonary Edema PLM010
Pulmonary Edema of Mountaineers PLM061
Pulmonary Embolism PLM033
Pulmonary Embolism and Infarction PLM027
Pulmonary Emphysema PLM034
Pulmonary Eosinophilia PLM035
Pulmonary Fibrosis PLM036
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 1 PLM139
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 PLM175
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 3 PLM143
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 4 PLM141
Pulmonary Fibrosis-Hepatic Hyperplasia-Bone Marrow Hypoplasia Syndrome PLM145
Pulmonary Fibrosis, Familial PLM044
Pulmonary Fibrosis, Idiopathic PLM134
Pulmonary Fungal Infections in Patients Deemed at Risk PLM107
Pulmonary Hemosiderosis PLM085
Pulmonary Hyalinizing Granuloma PLM062
Pulmonary Hypertension PLM037
Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis PLM101
Pulmonary Hypertension, Neonatal PLM124
Pulmonary Hypertension, Primary, 1 PLM164
Pulmonary Hypertension, Primary, 2 PLM128
Pulmonary Hypertension, Primary, 3 PLM127
Pulmonary Hypertension, Primary, 4 PLM121
Pulmonary Hypertension, Primary, Autosomal Recessive PLM169
Pulmonary Hypoplasia Familial Primary PLM063
Pulmonary Immaturity PLM013
Pulmonary Interstitial Glycogenosis PLM108
Pulmonary Large Cell Neuroendocrine Carcinoma PLM038
Pulmonary Neuroendocrine Tumor PLM039
Pulmonary Nodular Lymphoid Hyperplasia, Familial PLM153
Pulmonary Plasma Cell Granuloma PLM002
Pulmonary Sarcoidosis PLM012
Pulmonary Sclerosing Hemangioma PLM018
Pulmonary Sequestration PLM064
Pulmonary Subvalvular Stenosis PLM008
Pulmonary Supravalvular Stenosis PLM065
Pulmonary Surfactant Protein B, Deficiency of PLM066
Pulmonary Systemic Sclerosis PLM015
Pulmonary Tuberculosis PLM001
Pulmonary Type Ovarian Small Cell Carcinoma PLM024
Pulmonary Valve Agenesis-Intact Ventricular Septum-Persistent Ductus Arteriosus Syndrome PLM178
Pulmonary Valve Agenesis-Tetralogy of Fallot-Absence of Ductus Arteriosus Syndrome PLM157
Pulmonary Valve Disease PLM040
Pulmonary Valve Insufficiency PLM022
Pulmonary Valve Stenosis PLM041
Pulmonary Valves Agenesis PLM067
Pulmonary Vein Leiomyosarcoma PLM003
Pulmonary Vein Stenosis PLM068
Pulmonary Venoocclusive Disease PLM025
Pulmonary Venoocclusive Disease 1, Autosomal Dominant PLM170
Pulmonary Venoocclusive Disease 2, Autosomal Recessive PLM167
Pulmonary Venous Return Anomaly PLM069
Pulmonic Stenosis PLM070
Pulmonic Stenosis and Congenital Nephrosis PLM171
Pulmonic Stenosis and Deafness PLM166
Pulmonic Stenosis, Atrial Septal Defect, and Unique Electrocardiographic Abnormalities PLM165
Pulp Degeneration PLP002
Pulp Erosion PLP003
Pulpitis PLP001
Pulsating Exophthalmos PLS001
Punctate Acrokeratoderma Freckle Like Pigmentation PNC058
Punctate Epithelial Keratoconjunctivitis PNC012
Punctate Inner Choroidopathy PNC059
Punctate Palmoplantar Keratoderma PNC113
Punctate Porokeratosis PNC060
Pupil Disease PPL023
Pupil, Egg-Shaped PPL055
Pupillary Membrane, Persistence of PPL056
Pura Syndrome PRS125
Pura-Related Neurodevelopmental Disorders PRR032
Pure Autonomic Failure PRT058
Pure Mitochondrial Myopathy PRM138
Pure Red-Cell Aplasia PRR002
Purine Nucleoside Phosphorylase Deficiency PRN001
Purine-Pyrimidine Metabolic Disorder PRN024
Purpura PRP030
Purpura Fulminans PRP034
Purpura Simplex PRP069
Purulent Acute Otitis Media PRL012
Purulent Endophthalmitis PRL018
Purulent Labyrinthitis PRL001
Pustular Psoriasis PST059
Pustulosis of Palm and Sole PST011
Pustulosis Palmaris Et Plantaris PST062
Pycnodysostosis PYC001
Pyelitis PYL004
Pyelonephritis PYL005
Pyeloureteritis Cystica PYL001
Pyknoachondrogenesis PYK001
Pyle Disease PYL017
Pyloric Antrum Cancer PYL003
Pyloric Atresia PYL012
Pyloric Stenosis PYL006
Pyloric Stenosis, Infantile Hypertrophic, 1 PYL018
Pyloric Stenosis, Infantile Hypertrophic, 2 PYL008
Pyloric Stenosis, Infantile Hypertrophic, 3 PYL009
Pyloric Stenosis, Infantile Hypertrophic, 4 PYL010
Pyloric Stenosis, Infantile Hypertrophic, 5 PYL011
Pylorospasm PYL002
Pylorus Cancer PYL007
Pyoderma PYD002
Pyoderma Gangrenosum PYD001
Pyoderma Gangrenosum-Acne-Suppurative Hidradenitis Syndrome PYD004
Pyogenic Arthritis, Pyoderma Gangrenosum and Acne PYG002
Pyogenic Granuloma PYG006
Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne PYG003
Pyometritis PYM002
Pyomyositis PYM001
Pyosalpinx PYS001
Pyoureter PYR005
Pyridoxal 5'-Phosphate-Dependent Epilepsy PYR015
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency PYR021
Pyridoxine Deficiency PYR016
Pyridoxine Deficiency Anemia PYR009
Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia PYR007
Pyridoxine-Responsive Sideroblastic Anemia PYR006
Pyriform Sinus Cancer PYR008
Pyrimidine Metabolic Disorder PYR035
Pyromania PYR003
Pyropoikilocytosis, Hereditary PYR040
Pyruvate Carboxylase Deficiency PYR037
Pyruvate Dehydrogenase E1-Alpha Deficiency PYR022
Pyruvate Dehydrogenase E1-Beta Deficiency PYR012
Pyruvate Dehydrogenase E2 Deficiency PYR025
Pyruvate Dehydrogenase E3-Binding Protein Deficiency PYR031
Pyruvate Dehydrogenase Phosphatase Deficiency PYR018
Pyruvate Kinase Deficiency of Red Cells PYR041
Pyruvate Kinase Deficiency, Liver Type PYR019
Pyruvate Kinase Deficiency, Muscle Type PYR020
Pythiosis PYT001
Pyuria PYR004
Loading form....