Oxford University Press - Online Resource Centres

Young: 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