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Concept information

Preferred term

Meckel syndrome  

Definition(s)

  • Meckel syndrome is a rare, lethal, ciliopathic, genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations (occipital encephalocele), polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios. (Wikipedia)

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URI

http://data.loterre.fr/ark:/67375/VH8-JB5S9971-3

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