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EUROPLAN National Conference for Rare Diseases took place on 28-30 May 2010 in Plovdiv and received huge interest from medical professionals and patients (300 participants), official guests from EURORDIS and leading foreign experts on rare diseases were also present. The event was jointly organized by ICRDOD and NAPRD. During the conference the Bulgarian National Plan for Rare Diseases (2009-2013) and EUROPLAN recommendations for effective rare diseases strategies were officially presented to the Bulgarian rare diseases stakeholders. The results from the first Bulgarian epidemiological registry for rare diseases, the one of patients with thalassemia, were also made public during the event.
Description: ————————————————————————— SYNONIMS: Hepatolenticular degeneration ICD10 code: E83.0 ORPHANET number: ORPHA905 For more information about this disease, please visit the Orphanet website. RARE DISEASES LIBRARY: You may find a detailed description of Wilson disease in Issue 5 of “Rare Diseases & Orphan Drugs”. Click here to open the pdf-file (file size 690 KB). You can subscribe for our free e-newsletter by entering your e-mail here. ————————————————————————— SYNONIMS: – ICD10 code: Q93.8 ORPHANET number: ORPHA904 For more information about this disease, please visit the Orphanet website. ————————————————————————— SYNONIMS: Intestinal lipodystrophy ICD10 code: K90.8, M14.8 ORPHANET number: ORPHA3452 For more information about this disease, please visit the . ————————————————————————— SYNONIMS: – ICD10 code: М31.3 ORPHANET number: ORPHA900 For more information about this disease, please visit the Orphanet website. ————————————————————————— SYNONIMS: Torticollis spastica ICD10 code: – ORPHANET number: ORPHA93962 For more information about this disease, please visit the Orphanet website. ————————————————————————— SYNONIMS: Thalassaemia mayor also is known as Cooley anaemia or Mediterranean anemia ICD10 code: D56.1 ORPHANET number: ORPHA848 For more information about this disease, please visit the Orphanet website. ————————————————————————— SYNONIMS: Human nude/SCID (severe combined immunodeficiency) ICD10 code: D82.8 ORPHANET number: ORPHA169095 For more information about this disease, please visit the Orphanet website. —————————————————————————
The Fifth Eastern European Conference for Rare Diseases and Orphan Drugs “Rare Diseases in the Focus of Personalized Medicine” was organized together by BAPES and of the event
Last modification: 10:54 07.10.2010
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Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 13:49 18.08.2010
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Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 13:57 23.05.2024
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Last modification: 13:59 18.08.2010
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Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 12:19 18.08.2010
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Spasmodic torticollis
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 13:38 18.08.2010
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Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 13:54 22.05.2024
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Congenital alopecia and nail dystrophy associated with severe T-cell immunodeficiency
Visitors from North America may also contact NIH Office of Rare Diseases Research website.
Last modification: 13:57 22.05.2024
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