projects
SYNONIMS: –
ICD10 code: G71.0
ORPHANET number: ORPHA98896
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
RARE DISEASES LIBRARY:
You may find a detailed description of Duchenne Muscular Dystrophy in Issue 14 of “Rare Diseases & Orphan Drugs”. Click here to open the pdf-file (file size 690 KB).
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Last modification: 15:26 07.03.2013
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SYNONIMS:
White spot disease
Аcquired leukoderma
Depigmented skin
ICD10 code: L80
ORPHANET number: ORPHA3435
For more information about this disease, please visit the Orphanet website.
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
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Last modification: 13:52 18.08.2010
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This is a list of 6073 rare conditions (diseases and syndromes), compiled from different information sources (Orphanet, NORD etc.). It is not exhaustive, but can be used for educational and illustrative purposes.
Download the list of rare diseases – click
SYNONIMS: Progressive hemifacial atrophy ICD10 code: L94.8 ORPHANET number: ORPHA1214 For more information about this disease, please visit the . ————————————————————————— SYNONIMS: Male Turner Syndrome ICD10 code: Q87.1 ORPHANET number: ORPHA648 For more information about this disease, please visit the Orphanet website. ————————————————————————— SYNONIMS: Corticotroph pituitary adenoma ICD10 code: E24.0 ORPHANET number: ORPHA96253 For more information about this disease, please visit the Orphanet website. ————————————————————————— SYNONIMS: Charcot-Marie-Tooth hereditary neuropathy ICD10 code: G60.0 ORPHANET number: ORPHA166 For more information about this disease, please visit the Orphanet website. ————————————————————————— PREVALENCE OF RARE DISEASES: • National registry of patients with thalassemia major in Bulgaria • National registry of patients with chronic myeloid leukemia (CML) in Bulgaria • Pilot epidemiological study of chronic myeloid leukemia (CML) (click here for more information) RARE DISEASES WITHIN THE BULGARIAN PUBLIC HELATH SYSTEM: • Review of the actual situation and tendences in the rare diseases field in Bulgaria ORPHAN DRUGS: • Review of the access to orphan drugs in Bulgaria
Last modification: 10:47 28.08.2010
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Female Pseudo-Turner Syndrome
Turner Phenotype With Normal Karyotype
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 11:11 28.08.2010
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Primary pigmented nodular adrenal disease
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 06:35 29.08.2010
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Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 06:40 29.08.2010
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_____Information at the beginning of the project (August 2008)
_____Certification of BAPES as personal data administrator by the State Agency for Data Privacy Protection (October 2009)
_____Preliminary results (January 2010)
_____Phase I official results (April 2010)
_____Phase II official results (October 2010)
_____Phase I official results (November 2010)
_____issue 1 / November 2010 (click here to read the PDF file, 0.98 MB)
_____issue 1 / June 2010 (click here to read the PDF file, 150 KB)
_____issue 2 / March 2011 (click here to read the PDF file, 705 KB)