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- Roussy–Lévy_syndrome abstract "Roussy–Lévy syndrome, also known as Roussy–Lévy hereditary areflexic dystasia, is a rare genetic disorder of humans that results in progressive muscle wasting. It is caused by mutations in the genes that code for proteins necessary for the functioning of the myelin sheath of the neurons, affecting the conductance of nerve signals and resulting in loss of muscles' ability to move.The condition affects people from infants through adults and is inherited in an autosomal dominant manner. Currently, no cure is known for the disorder.".
- Roussy–Lévy_syndrome wikiPageID "36308777".
- Roussy–Lévy_syndrome wikiPageRevisionID "595351403".
- Roussy–Lévy_syndrome icd "334.3".
- Roussy–Lévy_syndrome icd "G60.0".
- Roussy–Lévy_syndrome name "Roussy–Lévy syndrome".
- Roussy–Lévy_syndrome omim "180800".
- Roussy–Lévy_syndrome subject Category:Autosomal_dominant_disorders.
- Roussy–Lévy_syndrome subject Category:Neurogenetic_disorders.
- Roussy–Lévy_syndrome type Disease.
- Roussy–Lévy_syndrome type Situation.
- Roussy–Lévy_syndrome comment "Roussy–Lévy syndrome, also known as Roussy–Lévy hereditary areflexic dystasia, is a rare genetic disorder of humans that results in progressive muscle wasting. It is caused by mutations in the genes that code for proteins necessary for the functioning of the myelin sheath of the neurons, affecting the conductance of nerve signals and resulting in loss of muscles' ability to move.The condition affects people from infants through adults and is inherited in an autosomal dominant manner.".
- Roussy–Lévy_syndrome label "Roussy–Lévy syndrome".
- Roussy–Lévy_syndrome sameAs Roussy%E2%80%93L%C3%A9vy_syndrome.
- Roussy–Lévy_syndrome sameAs Q7371349.
- Roussy–Lévy_syndrome sameAs Q7371349.
- Roussy–Lévy_syndrome wasDerivedFrom Roussy–Lévy_syndrome?oldid=595351403.