Welcome to biology-online.org! Please login to access all site features. Create account.
Log me on automatically each visit
| Page history
| Printable version
(Science: syndrome) An inherited type of heart disease where there are defects in the internal walls (septa) between the atrium and ventricle chambers of the heart.
holt-oram syndrome is dominant (requires only one copy in the genome to be expressed) and is often associated with skeletal deformities such as abnormally short forearms or thumbs.
Inheritance: autosomal dominant.
Please contribute to this project, if you have more information about this term feel free to edit this page
This page was last modified 21:16, 3 October 2005. This page has been accessed 782 times. What links here
| Related changes
| Permanent link
© Biology-Online.org. All Rights Reserved.
Register | Login
| About Us | Contact Us | Link to Us | Disclaimer & Privacy | Powered by CASPION