Young: Medical Genetics 
Multiple Choice QuestionsYoung: Medical Genetics
OMIM Database Links
OMIM™ - Online Mendelian Inheritance in Man™ - is a catalog database of human genes and genetic disorders.
Below is a list of the OMIM references throughout Medical Genetics along with a direct link to the OMIM entry.
| OMIM™ code | Medical Genetics page reference |
Disease | Web address |
| MIM 143100 | p.105 |
Huntington | www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143100 |
| MIM 154700 | p.106 |
Marfan syndrome | www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154700 |
| MIM 219700 | p.107 |
Cystic fibrosis | www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=219700 |
| MIM 265800 | p.108 |
Pyknodysostosis | www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=265800 |
| MIM 310200 | p.109 |
Duchenne muscular dystrophy | www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310200 |
| MIM 309550 | p.112 |
Fragile X syndrome | www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309550 |
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