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Whyte Murphy Syndrome: Disease Bioinformatics
Whyte-Murphy syndrome is characterized by the association of osteopathia striata (longitudinal striations about 2- to 3-mm-thick through most of the long bones, and only visible by radiographic examination) with a macular, hyperpigmented dermopathy and a white forelock. X-linked or autosomal dominant inheritance of Whyte-Murphy Syndrome is proposed. Osteopathia striata is asymptomatic accepting for some occasional joint discomfort. Treatment for Whyte-Murphy Syndrome includes external treatment for hyperpigmentation symptoms.
Whyte Murphy Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Whyte Murphy Syndrome below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
Whyte Murphy Syndrome has been studied in relation to diseases such as:
Alternate NamesWhyte Murphy Syndrome is also known as Osteopathia Striata Associated With Familial Dermopathy And White Forelock.