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Medword Medical Transcription NORD Rare Diseases ~H Medword Medical Transcription

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.

|5|A|B|C|D|E|F|G|H|I|J|K|L|M|
|N|O|P|Q|R|S|T|U|V|W|X|Y|Z|
Find on this page
H
Hageman Factor Deficiency
Hajdu Cheney Syndrome
Hallermann Streiff syndrome
Hallervorden Spatz Disease
Hand Foot Mouth Syndrome
Hanhart Syndrome
Hantavirus Pulmonary Syndrome
Hartnup Disease
Hashimoto's Syndrome
Hay Well's Syndrome
Headache, Cluster
Heart Block, Congenital
Heavy Metal Poisoning
Hemangioma Thrombocytopenia Syndrome
Hematuria, Benign, Familial
Hemochromatosis, Hereditary
Hemoglobinuria, Paroxysmal Cold
Hemoglobinuria, Paroxysmal Nocturnal
Hemolytic Uremic Syndrome
Hemophilia
Hemorrhagic Telangiectasia, Hereditary
Hepatic Fibrosis, Congenital
Hepatitis B
Hepatitis C
Hepatitis, Neonatal
Hepatorenal Syndrome
Hermansky Pudlak Syndrome
Hermaphroditism, True
Herpes, Neonatal
Hers Disease
Hiccups, Chronic
Hidradenitis Suppurativa
Hirschsprung's Disease
Histidinemia
Histiocytosis X
Hodgkin's Disease
Holoprosencephaly
Holt Oram Syndrome
Homocystinuria
Horner's Syndrome
Human Granulocytic Ehrlichiosis (HGE)
Human Monocytic Ehrlichiosis (HME)
Hunter Syndrome
Huntington's Disease
Hurler Syndrome
Hutchinson Gilford Progeria Syndrome
Hydranencephaly
Hydrocephalus
Hyper IgM Syndrome
Hypercholesterolemia
Hyperchylomicronemia
Hyperemesis Gravidarum
Hyperemesis Gravidarum
Hyperexplexia
Hyperhidrosis, Primary
Hyperkalemia
Hyperlipoproteinemia Type IV
Hyperostosis Frontalis Interna
Hyperoxaluria, Primary (Type I)
Hyperprolinemia Type I
Hyperprolinemia Type II
Hyperthermia
Hypochondroplasia
Hypoglycemia
Hypohidrotic Ectodermal Dysplasia
Hypokalemia
Hypomelanosis of Ito
Hypoparathyroidism
Hypophosphatasia
Hypoplastic Left Heart Syndrome
Hypotension, Orthostatic
Hypothyroidism
Hypotonia, Benign Congenital

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 Medword Medical Sales 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 NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions are strictly prohibited.


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