About: Oculoauricular syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Oculoauricular syndrome is a rare genetic condition affecting the eyes and ears. It is due to mutations in the (HMX1) gene. It is also known as the Schorderet-Munier-Franceschetti syndrome.

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dbo:abstract	Oculoauricular syndrome is a rare genetic condition affecting the eyes and ears. It is due to mutations in the (HMX1) gene. It is also known as the Schorderet-Munier-Franceschetti syndrome. (en)
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dbp:caption	Oculoauricular syndrome is inherited in an autosomal recessive manner. (en)
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rdfs:comment	Oculoauricular syndrome is a rare genetic condition affecting the eyes and ears. It is due to mutations in the (HMX1) gene. It is also known as the Schorderet-Munier-Franceschetti syndrome. (en)
rdfs:label	Oculoauricular syndrome (en)
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