Hereditary North American Indian childhood cirrhosis (Q43605): Difference between revisions
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CID11:DB93.20 | |||||||||||||||
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dki-india-DB93.20 | |||||||||||||||
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13 August 2026
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Latest revision as of 10:41, 13 August 2026
Hereditary North American Indian childhood cirrhosis is a severe autosomal recessive intrahepatic cholestasis that has only been described in aboriginal children from northwestern Quebec. Manifesting first as transient neonatal jaundice, the disease evolves into periportal fibrosis and cirrhosis during a period ranging from childhood to adolescence.
| Language | Label | Description | Also known as |
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| default for all languages | DB93.20 |
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| English | Hereditary North American Indian childhood cirrhosis |
Hereditary North American Indian childhood cirrhosis is a severe autosomal recessive intrahepatic cholestasis that has only been described in aboriginal children from northwestern Quebec. Manifesting first as transient neonatal jaundice, the disease evolves into periportal fibrosis and cirrhosis during a period ranging from childhood to adolescence. |
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CID11:DB93.20
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dki-india-DB93.20
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Concluído
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13 August 2026
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