Hereditary North American Indian childhood cirrhosis (Q43605): Difference between revisions
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Cirrose hereditária infantil de índios norte-americanos é uma colestase intrahepática autossômica recessiva grave que tem sido descrita apenas em crianças aborígenes do noroeste de Quebec. Manifesta-se primeiro como uma icterícia transitória neonatal, evoluindo para fibrose periportal e cirrose durante o período entre a infância até a adolescência. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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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| Property / Canonical URI: https://id.who.int/icd/entity/1992710077 / rank | |||||||||||||||
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CID11:DB93.20 | |||||||||||||||
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dki-india-DB93.20 | |||||||||||||||
| Property / Canary Token: dki-india-DB93.20 / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: K74 / rank | |||||||||||||||
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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 |
|---|---|---|---|
| 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. |
Statements
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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