Part,  Chapter, Paragraph

 1   II,     5.  5.  3| respectively (Nath et al, 2005; Orphanet, 2007; Vanacore, 2005).~
 2   II,     5.  5.  3|       Relat Disord 10(1):19-21.~Orphanet (2007): Prävalenzen seltener
 3   II,     5. 15.  2|         rare diseases: OMIM and Orphanet, plus a third database called
 4   II,     5. 15.  2|     several genetic diseases.~ ~Orphanet is a database of rare diseases
 5   II,     5. 15.  2|        them. The RD included in Orphanet are not exclusively genetic
 6   II,     5. 15.  2|        RD of unknown aetiology (Orphanet, 2005). The definition of
 7   II,     5. 15.  2|   specific RD or a group of RD. Orphanet is tracing them. Currently
 8   II,     5. 15.  2|   resources can be accessed via Orphanet through a query by disease
 9   II,     5. 15.  2|         established in Italy.~ ~Orphanet is conducting a permanent
10   II,     5. 15.  2|        report accessible on the Orphanet website. It is updated twice
11   II,     5. 15.  2|         not publicly available. Orphanet lists 250 registries in
12   II,     5. 15.  3|       Of the 5,000 RD listed in Orphanet, only 105 have a prevalence
13   II,     5. 15.  3|     still unknown. According to Orphanet 1,360 diseases can be diagnosed
14   II,     5. 15.  6|            accessed 08.05.2007)~Orphanet database of rare diseases
15  III,    10.  2.  4|    Co-operation and Development~Orphanet~European Database of Rare Diseases
16  III,    10.  2.  4|          European networks like Orphanet and EURORDIS and their respective
17  III,    10.  2.  4|      such as EGAN, EURORDIS and Orphanet are addressing the special