Kindler syndrome
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary",) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.
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Acrokeratotic poikilodermaBullous acrokeratotic poikiloderma of Kindler and WearyCongenital poikiloderma with blisters and keratosesCongenital poikiloderma with bullae and progressive cutaneous atrophyHereditary acrokeratotic poikilodermaHyperkeratosis-hyperpigmentation syndromeHyperkeratosis–hyperpigmentation syndromeKindler's syndromeKindler-Weary syndromeKindler–Weary syndromePoikiloderma congenital with bullae Weary typePoikiloderma hereditary acrokeratotic Weary typePoikiloderma of KindlerWeary-Kindler syndromeWeary–Kindler syndrome
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Acrokeratotic poikilodermaBullous acrokeratotic poikiloderma of Kindler and WearyCongenital poikiloderma with blisters and keratosesCongenital poikiloderma with bullae and progressive cutaneous atrophyEpidermolysis bullosaFERMT3GenodermatosisHereditary acrokeratotic poikilodermaHyperkeratosis-hyperpigmentation syndromeHyperkeratosis–hyperpigmentation syndromeKeratodermaKindlerKindler's syndromeKindler-Weary syndromeKindler–Weary syndromeList of OMIM disorder codesList of diseases (P)List of genes mutated in cutaneous conditionsList of skin conditionsList of syndromesPhotosensitivity in humansPoikilodermaPoikiloderma congenital with bullae Weary typePoikiloderma hereditary acrokeratotic Weary typePoikiloderma of KindlerPoikiloderma vasculare atrophicansUltravioletWeary-Kindler syndromeWeary–Kindler syndrome
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Kindler syndrome
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary",) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene.
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Kindler syndrome (also known a ...... a mutation in the KIND1 gene.
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La sindrome di Kindler o sindr ...... el gruppo delle genodermatosi.
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DiseasesDB
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derm
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eMedicine topic
943
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992,684,040
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Kindler syndrome has an autosomal recessive pattern of inheritance.
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DiseasesDB
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derm
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eMedicineTopic
ICD
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Q82.8
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Kindler syndrome
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OMIM
Orphanet
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Congenital poikiloderma with b ...... oderma, Weary–Kindler syndrome
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Kindler syndrome (also known a ...... a mutation in the KIND1 gene.
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La sindrome di Kindler o sindr ...... el gruppo delle genodermatosi.
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label
Kindler syndrome
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Kindler-Syndrom
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Sindrome di Kindler
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Kindler syndrome
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