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- Craniometaphyseal_dysplasia_autosomal_dominant abstract "Craniometaphyseal Dysplasia Autosomal Dominant is a disorder is a rare skeletal disorder that results from a heterozygous mutation in human homologous of progress in ankylosis gene (ANKH). Abnormal bone overgrowth occurs from the beginning of a child's life as well as throughout their lifetime resulting in the narrowing of the cranial formania.This leads to cranial nerve and facial features compression. In addition, this disorder is located on the 5p chomsome.".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageExternalLink ghr.nlm.nih.gov.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageExternalLink www.ncbi.nlm.nih.gov.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageExternalLink www.omim.org.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageID "46424372".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageLength "3170".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageOutDegree "4".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageRevisionID "697203324".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLink Category:Genetic_disease.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLink Category:Human_diseases_and_disorders.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLink Disease.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLink Mutation.
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLinkText "Craniometaphyseal dysplasia autosomal dominant".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLinkText "Craniometaphyseal dysplasia".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageWikiLinkText "craniometaphyseal dysplasia".
- Craniometaphyseal_dysplasia_autosomal_dominant wikiPageUsesTemplate Template:Reflist.
- Craniometaphyseal_dysplasia_autosomal_dominant subject Category:Genetic_disease.
- Craniometaphyseal_dysplasia_autosomal_dominant subject Category:Human_diseases_and_disorders.
- Craniometaphyseal_dysplasia_autosomal_dominant hypernym Disorder.
- Craniometaphyseal_dysplasia_autosomal_dominant type Disease.
- Craniometaphyseal_dysplasia_autosomal_dominant comment "Craniometaphyseal Dysplasia Autosomal Dominant is a disorder is a rare skeletal disorder that results from a heterozygous mutation in human homologous of progress in ankylosis gene (ANKH). Abnormal bone overgrowth occurs from the beginning of a child's life as well as throughout their lifetime resulting in the narrowing of the cranial formania.This leads to cranial nerve and facial features compression. In addition, this disorder is located on the 5p chomsome.".
- Craniometaphyseal_dysplasia_autosomal_dominant label "Craniometaphyseal dysplasia autosomal dominant".
- Craniometaphyseal_dysplasia_autosomal_dominant sameAs Q20790540.
- Craniometaphyseal_dysplasia_autosomal_dominant sameAs Kraniometaphysäre_Dysplasie.
- Craniometaphyseal_dysplasia_autosomal_dominant sameAs m.0134d0g9.
- Craniometaphyseal_dysplasia_autosomal_dominant sameAs Q20790540.
- Craniometaphyseal_dysplasia_autosomal_dominant wasDerivedFrom Craniometaphyseal_dysplasia_autosomal_dominant?oldid=697203324.
- Craniometaphyseal_dysplasia_autosomal_dominant homepage www.omim.org.
- Craniometaphyseal_dysplasia_autosomal_dominant isPrimaryTopicOf Craniometaphyseal_dysplasia_autosomal_dominant.