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- Jackson–Weiss_syndrome abstract "Jackson–Weiss syndrome (JWS) is a genetic disorder characterized by foot abnormalities and the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. It can also cause mental retardation and sometimes crossed eyes as well.It was characterized in 1976.".
- Jackson–Weiss_syndrome wikiPageID "3443488".
- Jackson–Weiss_syndrome wikiPageRevisionID "591878885".
- Jackson–Weiss_syndrome diseasesdb "31364".
- Jackson–Weiss_syndrome name "Jackson–Weiss syndrome".
- Jackson–Weiss_syndrome omim "123150".
- Jackson–Weiss_syndrome subject Category:Autosomal_dominant_disorders.
- Jackson–Weiss_syndrome subject Category:Cell_surface_receptor_deficiencies.
- Jackson–Weiss_syndrome subject Category:Rare_diseases.
- Jackson–Weiss_syndrome subject Category:Syndromes.
- Jackson–Weiss_syndrome type Disease.
- Jackson–Weiss_syndrome type Situation.
- Jackson–Weiss_syndrome comment "Jackson–Weiss syndrome (JWS) is a genetic disorder characterized by foot abnormalities and the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. It can also cause mental retardation and sometimes crossed eyes as well.It was characterized in 1976.".
- Jackson–Weiss_syndrome label "Jackson–Weiss syndrome".
- Jackson–Weiss_syndrome label "Zespół Jacksona-Weissa".
- Jackson–Weiss_syndrome sameAs Jackson%E2%80%93Weiss_syndrome.
- Jackson–Weiss_syndrome sameAs Zespół_Jacksona-Weissa.
- Jackson–Weiss_syndrome sameAs Q6118062.
- Jackson–Weiss_syndrome sameAs Q6118062.
- Jackson–Weiss_syndrome wasDerivedFrom Jackson–Weiss_syndrome?oldid=591878885.