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DeCS
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Descriptor English:
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Gilbert Disease
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Descriptor Spanish:
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Enfermedad de Gilbert
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Descriptor Portuguese:
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Doença de Gilbert
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Tree Number:
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C16.320.565.300.528
C18.452.648.300.528
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Definition English:
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A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. |
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History Note English:
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2000(1975)
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Allowable Qualifiers English:
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Record Number:
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6017
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Unique Identifier:
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D005878
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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