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- Coffin–Lowry_syndrome abstract "Coffin–Lowry syndrome is a genetic disorder that is X-linked dominant and which causes severe mental problems sometimes associated with abnormalities of growth, cardiac abnormalities, kyphoscoliosis, as well as auditory and visual abnormalities.".
- Coffin–Lowry_syndrome wikiPageExternalLink clsf.info.
- Coffin–Lowry_syndrome wikiPageExternalLink ghr.nlm.nih.gov.
- Coffin–Lowry_syndrome wikiPageExternalLink coffin-lowry-syndrome.
- Coffin–Lowry_syndrome wikiPageExternalLink br.fcgi?book=gene&part=cls.
- Coffin–Lowry_syndrome wikiPageExternalLink index.htm.
- Coffin–Lowry_syndrome wikiPageExternalLink symptoms.htm.
- Coffin–Lowry_syndrome wikiPageID "1492806".
- Coffin–Lowry_syndrome wikiPageLength "5723".
- Coffin–Lowry_syndrome wikiPageOutDegree "16".
- Coffin–Lowry_syndrome wikiPageRevisionID "677388999".
- Coffin–Lowry_syndrome wikiPageWikiLink Category:Deficiencies_of_intracellular_signaling_peptides_and_proteins.
- Coffin–Lowry_syndrome wikiPageWikiLink Category:Rare_diseases.
- Coffin–Lowry_syndrome wikiPageWikiLink Category:Syndromes.
- Coffin–Lowry_syndrome wikiPageWikiLink Cell_signaling.
- Coffin–Lowry_syndrome wikiPageWikiLink Gene.
- Coffin–Lowry_syndrome wikiPageWikiLink Genetic_disorder.
- Coffin–Lowry_syndrome wikiPageWikiLink Kyphoscoliosis.
- Coffin–Lowry_syndrome wikiPageWikiLink ERK_pathway.
- Coffin–Lowry_syndrome wikiPageWikiLink MAPK_signaling_pathway.
- Coffin–Lowry_syndrome wikiPageWikiLink Microcephaly.
- Coffin–Lowry_syndrome wikiPageWikiLink Micrognathia.
- Coffin–Lowry_syndrome wikiPageWikiLink Micrognathism.
- Coffin–Lowry_syndrome wikiPageWikiLink Mutation.
- Coffin–Lowry_syndrome wikiPageWikiLink Protein.
- Coffin–Lowry_syndrome wikiPageWikiLink RPS6KA3.
- Coffin–Lowry_syndrome wikiPageWikiLink Sex_linkage.
- Coffin–Lowry_syndrome wikiPageWikiLink X-linked.
- Coffin–Lowry_syndrome wikiPageWikiLink X-linked_dominant.
- Coffin–Lowry_syndrome wikiPageWikiLink X-linked_dominant_inheritance.
- Coffin–Lowry_syndrome wikiPageWikiLink X_chromosome.
- Coffin–Lowry_syndrome wikiPageWikiLinkText "Coffin–Lowry syndrome".
- Coffin–Lowry_syndrome diseasesdb "2934".
- Coffin–Lowry_syndrome hasPhotoCollection Coffin–Lowry_syndrome.
- Coffin–Lowry_syndrome icd "759.89".
- Coffin–Lowry_syndrome icd "Q87.8".
- Coffin–Lowry_syndrome meshid "D038921".
- Coffin–Lowry_syndrome name "Coffin–Lowry syndrome".
- Coffin–Lowry_syndrome omim "303600".
- Coffin–Lowry_syndrome wikiPageUsesTemplate Template:Deficiencies_of_intracellular_signaling_peptides_and_proteins.
- Coffin–Lowry_syndrome wikiPageUsesTemplate Template:Infobox_Disease.
- Coffin–Lowry_syndrome wikiPageUsesTemplate Template:Reflist.
- Coffin–Lowry_syndrome wikiPageUsesTemplate Template:X-linked_disorders.
- Coffin–Lowry_syndrome subject Category:Deficiencies_of_intracellular_signaling_peptides_and_proteins.
- Coffin–Lowry_syndrome subject Category:Rare_diseases.
- Coffin–Lowry_syndrome subject Category:Syndromes.
- Coffin–Lowry_syndrome comment "Coffin–Lowry syndrome is a genetic disorder that is X-linked dominant and which causes severe mental problems sometimes associated with abnormalities of growth, cardiac abnormalities, kyphoscoliosis, as well as auditory and visual abnormalities.".
- Coffin–Lowry_syndrome label "Coffin–Lowry syndrome".
- Coffin–Lowry_syndrome sameAs Coffin-Lowry-Syndrom.
- Coffin–Lowry_syndrome sameAs Síndrome_de_Coffin-Lowry.
- Coffin–Lowry_syndrome sameAs Syndrome_de_Coffin-Lowry.
- Coffin–Lowry_syndrome sameAs Sindrome_di_Coffin-Lowry.
- Coffin–Lowry_syndrome sameAs Sindrom_Coffin-Lowry.
- Coffin–Lowry_syndrome sameAs Zespxc3xb3xc5x82_Coffina-Lowryego.
- Coffin–Lowry_syndrome sameAs m.055m_g.
- Coffin–Lowry_syndrome sameAs Q1106881.
- Coffin–Lowry_syndrome sameAs Q1106881.
- Coffin–Lowry_syndrome sameAs 科芬-勞里症候群.
- Coffin–Lowry_syndrome wasDerivedFrom Coffin–Lowry_syndrome?oldid=677388999.
- Coffin–Lowry_syndrome isPrimaryTopicOf Coffin–Lowry_syndrome.