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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 28/08/2006 |
Symbol | OPM |
Location | 7q21.3 |
Name | osteoporosis, postmenopausal |
Corresponding gene | COL1A2 |
Main clinical features | severe osteopenia |
Genetic determination | other |
Function/system disorder | osteo-articular |
connective tissue | |
Type | disease |
Remark(s) | gly661-to-ser mutation in the COL1A2 gene |