Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/ABCD_syndrome> ?p ?o }
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- ABCD_syndrome abstract "ABCD syndrome is the acronym for albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness. It has been found to be caused by mutation in the endothelin B receptor gene (EDNRB).".
- ABCD_syndrome omim "600501".
- ABCD_syndrome thumbnail Patient_with_Waardenburg-Klein_syndrome_(1916).jpg?width=300.
- ABCD_syndrome wikiPageExternalLink OMIM.
- ABCD_syndrome wikiPageExternalLink carddisp?gene=EDNRB.
- ABCD_syndrome wikiPageID "3062597".
- ABCD_syndrome wikiPageLength "13972".
- ABCD_syndrome wikiPageOutDegree "27".
- ABCD_syndrome wikiPageRevisionID "703051558".
- ABCD_syndrome wikiPageWikiLink Acronym.
- ABCD_syndrome wikiPageWikiLink Albinism.
- ABCD_syndrome wikiPageWikiLink Autoimmune_disease.
- ABCD_syndrome wikiPageWikiLink Blaschkos_lines.
- ABCD_syndrome wikiPageWikiLink Category:Cell_surface_receptor_deficiencies.
- ABCD_syndrome wikiPageWikiLink Category:Disturbances_of_human_pigmentation.
- ABCD_syndrome wikiPageWikiLink Category:Rare_diseases.
- ABCD_syndrome wikiPageWikiLink Category:Syndromes.
- ABCD_syndrome wikiPageWikiLink DNA.
- ABCD_syndrome wikiPageWikiLink Depigmentation.
- ABCD_syndrome wikiPageWikiLink Endothelin_receptor_type_B.
- ABCD_syndrome wikiPageWikiLink Gel_electrophoresis.
- ABCD_syndrome wikiPageWikiLink Hearing_loss.
- ABCD_syndrome wikiPageWikiLink Hirschsprungs_disease.
- ABCD_syndrome wikiPageWikiLink List_of_cutaneous_conditions.
- ABCD_syndrome wikiPageWikiLink Melanocyte.
- ABCD_syndrome wikiPageWikiLink Mutation.
- ABCD_syndrome wikiPageWikiLink Neuron.
- ABCD_syndrome wikiPageWikiLink Petrus_Johannes_Waardenburg.
- ABCD_syndrome wikiPageWikiLink Photophobia.
- ABCD_syndrome wikiPageWikiLink Symptom.
- ABCD_syndrome wikiPageWikiLink Unibrow.
- ABCD_syndrome wikiPageWikiLink Waardenburg_syndrome.
- ABCD_syndrome wikiPageWikiLink Zygosity.
- ABCD_syndrome wikiPageWikiLinkText "ABCD syndrome".
- ABCD_syndrome caption "Facial morphology of Waardenburg syndrome, not type IV".
- ABCD_syndrome diseasesdb "33683".
- ABCD_syndrome name "ABCD syndrome".
- ABCD_syndrome omim "600501".
- ABCD_syndrome wikiPageUsesTemplate Template:Cell_surface_receptor_deficiencies.
- ABCD_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- ABCD_syndrome wikiPageUsesTemplate Template:Pigmentation_disorders.
- ABCD_syndrome wikiPageUsesTemplate Template:RareDiseases.
- ABCD_syndrome wikiPageUsesTemplate Template:Reflist.
- ABCD_syndrome wikiPageUsesTemplate Template:Research_help.
- ABCD_syndrome wikiPageUsesTemplate Template:Technical.
- ABCD_syndrome subject Category:Cell_surface_receptor_deficiencies.
- ABCD_syndrome subject Category:Disturbances_of_human_pigmentation.
- ABCD_syndrome subject Category:Rare_diseases.
- ABCD_syndrome subject Category:Syndromes.
- ABCD_syndrome hypernym Acronym.
- ABCD_syndrome type Company.
- ABCD_syndrome type Disease.
- ABCD_syndrome type Deficiency.
- ABCD_syndrome type Disorder.
- ABCD_syndrome type Redirect.
- ABCD_syndrome type Syndrome.
- ABCD_syndrome type Thing.
- ABCD_syndrome type Q12136.
- ABCD_syndrome comment "ABCD syndrome is the acronym for albinism, black lock, cell migration disorder of the neurocytes of the gut and sensorineural deafness. It has been found to be caused by mutation in the endothelin B receptor gene (EDNRB).".
- ABCD_syndrome label "ABCD syndrome".
- ABCD_syndrome sameAs Q3508565.
- ABCD_syndrome sameAs Síndrome_ABCD.
- ABCD_syndrome sameAs Syndrome_ABCD.
- ABCD_syndrome sameAs m.08nzs6.
- ABCD_syndrome sameAs Q3508565.
- ABCD_syndrome wasDerivedFrom ABCD_syndrome?oldid=703051558.
- ABCD_syndrome depiction Patient_with_Waardenburg-Klein_syndrome_(1916).jpg.
- ABCD_syndrome isPrimaryTopicOf ABCD_syndrome.
- ABCD_syndrome name "ABCD syndrome".