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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• Barth Syndome  + (Barth Syndome (BTHS) is an X-linked geneti … Barth Syndome (BTHS) is an X-linked genetic condition that is caused by a mutation in the tafazzin gene (taz). This mutation causes cardiolipin abnormalities, cardiomyopathy, neutropenia, muscle weakness, growth delay, and exercise intolerance.</br></br>[https://www.barthsyndrome.org/about-barth-syndrome/overview-of-barth-syndrome Weblink]</br> Contributed by [[Sparagna GC]] 2016-04-24[[Sparagna GC]] 2016-04-24)

• Barth Syndome  +