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- Yemenite_deaf-blind_hypopigmentation_syndrome abstract "The genetic disorder Yemenite deaf-blind hypopigmentation syndrome, also known as Warburg-Thomsen syndrome, is a condition caused by a mutation on the SRY-related HMG-box gene 10 (not SOX10).It was characterized in 1990, after being seen in two siblings from Yemen who presented with a \"hitherto undescribed association of microcornea, colobomata of the iris and choroidea, nystagmus, severe early hearing loss, and patchy hypo- and hyperpigmentation.\" Some sources affirm SOX10 involvement.".
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageID "24161257".
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageLength "3068".
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageOutDegree "5".
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageRevisionID "702185863".
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageWikiLink ABCD_syndrome.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageWikiLink Category:Disturbances_of_human_pigmentation.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageWikiLink List_of_cutaneous_conditions.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageWikiLink SOX10.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageWikiLink Yemen.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageWikiLinkText "Yemenite deaf-blind hypopigmentation syndrome".
- Yemenite_deaf-blind_hypopigmentation_syndrome name "Yemenite deaf-blind hypopigmentation syndrome".
- Yemenite_deaf-blind_hypopigmentation_syndrome omim "601706".
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageUsesTemplate Template:Cutaneous-condition-stub.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageUsesTemplate Template:Infobox_Disease.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageUsesTemplate Template:Reflist.
- Yemenite_deaf-blind_hypopigmentation_syndrome wikiPageUsesTemplate coregulator_deficiencies.
- Yemenite_deaf-blind_hypopigmentation_syndrome subject Category:Disturbances_of_human_pigmentation.
- Yemenite_deaf-blind_hypopigmentation_syndrome hypernym Condition.
- Yemenite_deaf-blind_hypopigmentation_syndrome type Disease.
- Yemenite_deaf-blind_hypopigmentation_syndrome type Thing.
- Yemenite_deaf-blind_hypopigmentation_syndrome type Q12136.
- Yemenite_deaf-blind_hypopigmentation_syndrome comment "The genetic disorder Yemenite deaf-blind hypopigmentation syndrome, also known as Warburg-Thomsen syndrome, is a condition caused by a mutation on the SRY-related HMG-box gene 10 (not SOX10).It was characterized in 1990, after being seen in two siblings from Yemen who presented with a \"hitherto undescribed association of microcornea, colobomata of the iris and choroidea, nystagmus, severe early hearing loss, and patchy hypo- and hyperpigmentation.\" Some sources affirm SOX10 involvement.".
- Yemenite_deaf-blind_hypopigmentation_syndrome label "Yemenite deaf-blind hypopigmentation syndrome".
- Yemenite_deaf-blind_hypopigmentation_syndrome sameAs Q8052144.
- Yemenite_deaf-blind_hypopigmentation_syndrome sameAs m.07kcrsp.
- Yemenite_deaf-blind_hypopigmentation_syndrome sameAs Q8052144.
- Yemenite_deaf-blind_hypopigmentation_syndrome wasDerivedFrom Yemenite_deaf-blind_hypopigmentation_syndrome?oldid=702185863.
- Yemenite_deaf-blind_hypopigmentation_syndrome isPrimaryTopicOf Yemenite_deaf-blind_hypopigmentation_syndrome.