This listing of rare diseases
is provided for spelling reference. Clicking on the link will generate a new
window and take you to NORD's home page, where you may search for an abstract of
the disease or order a full text report of the disease. Please read the notice
at the bottom of this page before using this list.
P Pachydermoperiostosis Paget's Disease Paget's Disease of the Breast Pallister Hall Syndrome Pallister Killian Mosaic Syndrome Pallister W Syndrome Pancreatic Islet Cell Tumor Panic Anxiety Syndrome Panniculitis, Idiopathic Nodular Papillitis Papillon Lefevre Syndrome Paracoccidioidomycosis Paramyotonia Congenita Paraplegia, Hereditary Spastic Parkinson's Disease Parry Romberg Syndrome Pars Planitis Parsonage Turner Syndrome Patulous Eustachian Tube Peeling Skin Syndrome Pelizaeus Merzbacher Brain Sclerosis Pemphigoid, Benign Mucosal Pemphigus Penta X Syndrome Pentalogy of Cantrell PEPCK Deficiency, Mitochondrial Perisylvian Syndrome, Congenital Bilateral Perniosis Pertussis Peutz Jeghers Syndrome Peyronie Disease Pfeiffer Syndrome Type I Phenylketonuria Pheochromocytoma Phocomelia Syndrome Phosphoglycerate Kinase Deficiency Pica Pick's Disease Pierre Robin Syndrome Pinta Pityriasis Rubra Pilaris Pneumonia, Eosinophilic Pneumonia, Interstitial POEMS Syndrome Poland Syndrome Polyarteritis Nodosa Polychondritis Polycystic Kidney Diseases Polycystic Liver Disease Polycythemia Vera Polyglucosan Body Disease, Adult Polymyalgia Rheumatica Polymyositis Polyposis, Familial Pompe Disease Popliteal Pterygium Syndrome Porphyria Porphyria Cutanea Tarda Porphyria, Acute Intermittent Porphyria, ALA-D Porphyria, Congenital Erythropoietic Porphyria, Hereditary Coproporphyria Porphyria, Variegate Post Polio Syndrome Posterior Uveitis Prader Willi Syndrome Precocious Puberty Primary Lateral Sclerosis Proctitis Progressive Osseous Heteroplasia (POH) Progressive Supranuclear Palsy Prostatitis Proteus Syndrome Prune Belly Syndrome Pseudo Hurler Polydystrophy Pseudocholinesterase Deficiency Pseudohypoparathyroidism Pseudomyxoma Peritonei Pseudotumor Cerebri Pseudoxanthoma Elasticum (PXE) Psittacosis Psoriasis Pterygium Syndrome, Multiple Pulmonary Alveolar Proteinosis Pulmonary Hypertension, Primary Pulmonary Hypertension, Secondary Pure Red Cell Aplasia, Acquired Purpura, Henoch Schonlein Purpura, Idiopathic Thrombocytopenic Purpura, Thrombotic Thrombocytopenic Pyknodysostosis Pyoderma Gangrenosum Pyruvate Carboxylase Deficiency Pyruvate Dehydrogenase Deficiency Pyruvate Kinase Deficiency
Please Click HERE for
a comma-delimited list of the rare diseases that you may add to your speller.
List made available
by express written permission of
NORD National Organization for Rare Disorders, Inc.
Important:
Please use the above list at your own risk. While we make every effort to ensure
accuracy, we cannot be held responsible for errors in spelling or capitalization,
or any circumstance that may result because of said error. In using the above list
you also agree to never hold ANSO Consulting Inc. or Canadian MT Medical Transcription
responsible for any errors should they exist.
Please Note:
The National Organization for Rare Disorders (NORD) web site, its databases, and
the contents thereof are copyrighted by NORD. No part of the NORD web site, databases,
or the contents may be copied in any way, including but not limited to the following:
electronically downloading, storing in a retrieval system, or redistributing for
any commercial purposes without the express written permission of NORD. Permission
is hereby granted to print one hard copy of the information on an individual disease
for your personal use, provided that such content is in no way modified, and that
credit for the source (NORD) and NORDs copyright notice are included on the
printed copy. Any other electronic reproduction or other printed versions are strictly
prohibited.
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