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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.
Vizit™, under license from BioVista Inc.

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Whyte Murphy Syndrome has been studied in relation to diseases such as:

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Alternate Names

Whyte Murphy Syndrome is also known as Osteopathia Striata Associated With Familial Dermopathy And White Forelock.