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- Kindler_syndrome abstract "Kindler syndrome (also known as "Bullous acrokeratotic poikiloderma of Kindler and Weary,", "Congenital poikiloderma with blisters and keratoses," "Congenital poikiloderma with bullae and progressive cutaneous atrophy," "Hereditary acrokeratotic poikiloderma," "Hyperkeratosis–hyperpigmentation syndrome," "Acrokeratotic poikiloderma," and "Weary–Kindler syndrome") is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.".
- Kindler_syndrome diseasesdb "32778".
- Kindler_syndrome emedicineSubject "derm".
- Kindler_syndrome emedicineTopic "943".
- Kindler_syndrome icd10 "Q82.8".
- Kindler_syndrome omim "173650".
- Kindler_syndrome thumbnail Autorecessive.svg?width=300.
- Kindler_syndrome wikiPageExternalLink kindler-syndrome.
- Kindler_syndrome wikiPageExternalLink kindler_syndrome.
- Kindler_syndrome wikiPageID "6725385".
- Kindler_syndrome wikiPageRevisionID "592124017".
- Kindler_syndrome diseasesdb "32778".
- Kindler_syndrome emedicinesubj "derm".
- Kindler_syndrome emedicinetopic "943".
- Kindler_syndrome hasPhotoCollection Kindler_syndrome.
- Kindler_syndrome icd "Q82.8".
- Kindler_syndrome name "Kindler syndrome".
- Kindler_syndrome omim "173650".
- Kindler_syndrome wordnet_type synset-disease-noun-1.
- Kindler_syndrome subject Category:Autosomal_recessive_disorders.
- Kindler_syndrome subject Category:Genodermatoses.
- Kindler_syndrome subject Category:Papulosquamous_hyperkeratotic_cutaneous_conditions.
- Kindler_syndrome subject Category:Rare_diseases.
- Kindler_syndrome type Abstraction100002137.
- Kindler_syndrome type Attribute100024264.
- Kindler_syndrome type AutosomalRecessiveDisorders.
- Kindler_syndrome type Condition113920835.
- Kindler_syndrome type Disease114070360.
- Kindler_syndrome type Disorder114052403.
- Kindler_syndrome type IllHealth114052046.
- Kindler_syndrome type Illness114061805.
- Kindler_syndrome type PapulosquamousHyperkeratoticCutaneousConditions.
- Kindler_syndrome type PathologicalState114051917.
- Kindler_syndrome type PhysicalCondition114034177.
- Kindler_syndrome type State100024720.
- Kindler_syndrome type Disease.
- Kindler_syndrome type AilmentCondition.
- Kindler_syndrome type Situation.
- Kindler_syndrome comment "Kindler syndrome (also known as "Bullous acrokeratotic poikiloderma of Kindler and Weary,", "Congenital poikiloderma with blisters and keratoses," "Congenital poikiloderma with bullae and progressive cutaneous atrophy," "Hereditary acrokeratotic poikiloderma," "Hyperkeratosis–hyperpigmentation syndrome," "Acrokeratotic poikiloderma," and "Weary–Kindler syndrome") is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.".
- Kindler_syndrome label "Kindler syndrome".
- Kindler_syndrome label "Kindler-Syndrom".
- Kindler_syndrome sameAs Kindler-Syndrom.
- Kindler_syndrome sameAs m.0gkrpg.
- Kindler_syndrome sameAs Q1741965.
- Kindler_syndrome sameAs Q1741965.
- Kindler_syndrome sameAs 645.
- Kindler_syndrome sameAs Kindler_syndrome.
- Kindler_syndrome wasDerivedFrom Kindler_syndrome?oldid=592124017.
- Kindler_syndrome depiction Autorecessive.svg.
- Kindler_syndrome isPrimaryTopicOf Kindler_syndrome.
- Kindler_syndrome name "Kindler syndrome".
