Matches in DBpedia 2014 for { <http://dbpedia.org/resource/ABCD_syndrome> ?p ?o. }
Showing items 1 to 63 of
63
with 100 items per page.
- 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 diseasesdb "33683".
- 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 wikiPageRevisionID "589913612".
- ABCD_syndrome caption "Facial morphology of Waardenburg syndrome, not type IV".
- ABCD_syndrome diseasesdb "33683".
- ABCD_syndrome hasPhotoCollection ABCD_syndrome.
- ABCD_syndrome name "ABCD syndrome".
- ABCD_syndrome omim "600501".
- ABCD_syndrome wordnet_type synset-disease-noun-1.
- 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 type Abstraction100002137.
- ABCD_syndrome type Act100030358.
- ABCD_syndrome type Activity100407535.
- ABCD_syndrome type Attribute100024264.
- ABCD_syndrome type CellSurfaceReceptorDeficiencies.
- ABCD_syndrome type Cognition100023271.
- ABCD_syndrome type Complex105870365.
- ABCD_syndrome type Concept105835747.
- ABCD_syndrome type Condition113920835.
- ABCD_syndrome type Content105809192.
- ABCD_syndrome type Disease114070360.
- ABCD_syndrome type DisturbancesOfHumanPigmentation.
- ABCD_syndrome type Event100029378.
- ABCD_syndrome type Idea105833840.
- ABCD_syndrome type IllHealth114052046.
- ABCD_syndrome type Illness114061805.
- ABCD_syndrome type Lack114449405.
- ABCD_syndrome type Need114449126.
- ABCD_syndrome type PathologicalState114051917.
- ABCD_syndrome type Perturbation107428450.
- ABCD_syndrome type PhysicalCondition114034177.
- ABCD_syndrome type PsychologicalFeature100023100.
- ABCD_syndrome type State100024720.
- ABCD_syndrome type Syndrome105870790.
- ABCD_syndrome type Syndromes.
- ABCD_syndrome type Whole105869584.
- ABCD_syndrome type YagoPermanentlyLocatedEntity.
- ABCD_syndrome type Disease.
- ABCD_syndrome type AilmentCondition.
- ABCD_syndrome type Situation.
- 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 label "Syndrome ABCD".
- ABCD_syndrome label "Síndrome ABCD".
- ABCD_syndrome sameAs Síndrome_ABCD.
- ABCD_syndrome sameAs Syndrome_ABCD.
- ABCD_syndrome sameAs m.08nzs6.
- ABCD_syndrome sameAs Q3508565.
- ABCD_syndrome sameAs Q3508565.
- ABCD_syndrome sameAs 12.
- ABCD_syndrome sameAs ABCD_syndrome.
- ABCD_syndrome wasDerivedFrom ABCD_syndrome?oldid=589913612.
- ABCD_syndrome depiction Patient_with_Waardenburg-Klein_syndrome_(1916).jpg.
- ABCD_syndrome isPrimaryTopicOf ABCD_syndrome.
- ABCD_syndrome name "ABCD syndrome".