Part,  Chapter, Paragraph

1   II,     5. 15.Acr|    Reference Centres Network~MIM~Mendelian Inheritance in Man~MS~Member
2   II,     5. 15.  2|        the Online version of the Mendelian Inheritance in Man. It is
3   II,     5. 15.  3|           Most rare diseases are mendelian genetic disorders and all
4   II,     5. 15.  3|        genetic disorders and all mendelian genetic disorders are rare
5   II,     5. 15.  3| dissemination. For what concerns mendelian genetic disorders, the MIM
6   II,     5. 15.  4|         sector will include rare mendelian phenotypes of common diseases.~ ~
7   II,     5. 15.  6|      1016-9.~McKusick VA (2007): Mendelian Inheritance in Man and its
8  III,    10.  2.  4|        either following mainly a mendelian trait (“inherited”) or mainly
9  III,    10.  2.  4|     complex diseases following a mendelian trait) and low or moderate