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- Crouzonodermoskeletal_syndrome abstract "Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.Some of the signs and symptoms of Crouzonodermoskeletal syndrome are similar to those seen with Crouzon syndrome. They include prematurely fused skull bones, which affect the shape of the head and face; wide-set, bulging eyes due to shallow eye sockets; eyes that do not point in the same direction (strabismus); a small, beaked nose; and an underdeveloped upper jaw. People with these conditions are generally of normal intelligence.Several features distinguish Crouzonodermoskeletal syndrome from Crouzon syndrome. People with Crouzonodermoskeletal syndrome have acanthosis nigricans, a skin condition characterized by thick, dark, velvety skin in body folds and creases, including the neck and underarms. In addition, subtle changes may be seen in the bones of the spine (vertebrae). Noncancerous growths called cementomas may develop in the jaw during young adulthood.Crouzonodermoskeletal syndrome is rare; the condition is seen in about 1 per million people.".
- Crouzonodermoskeletal_syndrome wikiPageID "3442595".
- Crouzonodermoskeletal_syndrome wikiPageLength "3745".
- Crouzonodermoskeletal_syndrome wikiPageOutDegree "13".
- Crouzonodermoskeletal_syndrome wikiPageRevisionID "626425361".
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Acanthosis_nigricans.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Bone.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Category:Congenital_disorders_of_musculoskeletal_system.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Category:Genetic_disorders_with_no_OMIM.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Cementoma.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Craniosynostosis.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Crouzon_syndrome.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink FGFR3.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Fibroblast_growth_factor_receptor_3.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Gene.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Human_skull.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Protein.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Strabismus.
- Crouzonodermoskeletal_syndrome wikiPageWikiLink Vertebra.
- Crouzonodermoskeletal_syndrome wikiPageWikiLinkText "Crouzonodermoskeletal syndrome".
- Crouzonodermoskeletal_syndrome hasPhotoCollection Crouzonodermoskeletal_syndrome.
- Crouzonodermoskeletal_syndrome wikiPageUsesTemplate Template:Cite_journal.
- Crouzonodermoskeletal_syndrome wikiPageUsesTemplate Template:OMIM.
- Crouzonodermoskeletal_syndrome wikiPageUsesTemplate Template:Reflist.
- Crouzonodermoskeletal_syndrome subject Category:Congenital_disorders_of_musculoskeletal_system.
- Crouzonodermoskeletal_syndrome subject Category:Genetic_disorders_with_no_OMIM.
- Crouzonodermoskeletal_syndrome hypernym Disorder.
- Crouzonodermoskeletal_syndrome type Disease.
- Crouzonodermoskeletal_syndrome type Disorder.
- Crouzonodermoskeletal_syndrome comment "Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.Some of the signs and symptoms of Crouzonodermoskeletal syndrome are similar to those seen with Crouzon syndrome.".
- Crouzonodermoskeletal_syndrome label "Crouzonodermoskeletal syndrome".
- Crouzonodermoskeletal_syndrome sameAs m.09cnjg.
- Crouzonodermoskeletal_syndrome sameAs Q5189052.
- Crouzonodermoskeletal_syndrome sameAs Q5189052.
- Crouzonodermoskeletal_syndrome wasDerivedFrom Crouzonodermoskeletal_syndrome?oldid=626425361.
- Crouzonodermoskeletal_syndrome isPrimaryTopicOf Crouzonodermoskeletal_syndrome.