Meckel-Gruber syndrome (Q46421): Difference between revisions
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Revision as of 14:59, 13 August 2026
Meckel syndrome (MKS) is a monogenic disease characterised by a combination of renal cysts and variably associated features, including developmental anomalies of the central nervous system (usually occipital encephalocele), hepatic ductal dysplasia and cysts, and polydactyly, and a lethal course, with death occurring in the perinatal period.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD2F.13 |
||
| English | Meckel-Gruber syndrome |
Meckel syndrome (MKS) is a monogenic disease characterised by a combination of renal cysts and variably associated features, including developmental anomalies of the central nervous system (usually occipital encephalocele), hepatic ductal dysplasia and cysts, and polydactyly, and a lethal course, with death occurring in the perinatal period. |
Statements
CID11:LD2F.13
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dki-india-LD2F.13
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Concluído
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13 August 2026
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