Cholestasis - lymphoedema syndrome (Q64269): Difference between revisions
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Latest revision as of 11:51, 14 August 2026
Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1087517390 |
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| English | Cholestasis - lymphoedema syndrome |
Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly. |
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CID11:ID_1087517390
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dki-india-ID_1087517390
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Concluído
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13 August 2026
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