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disease > congenital disease > malformation > polydactyly > Meckel syndrome
... > disease > congenital disease > malformation > dysostosis > polydactyly > Meckel syndrome
disease > diseases of the osteoarticular system > dysostosis > polydactyly > Meckel syndrome
disease > disease of the hand > polydactyly > Meckel syndrome
disease > genetic disease > hereditary disease > polycystic kidney > Meckel syndrome
disease > urinary system disease > kidney disease > polycystic kidney > Meckel syndrome
... > disease > tumor > benign neoplasm > cyst > polycystic kidney > Meckel syndrome
disease > digestive diseases > hepatic disease > hepatic fibrosis > Meckel syndrome
disease > connective tissue disease > fibrosis > hepatic fibrosis > Meckel syndrome
... > disease > systemic disease > connective tissue disease > fibrosis > hepatic fibrosis > Meckel syndrome
... > disease > nervous system diseases > central nervous system diseases > cerebral disorder > encephalocele > Meckel syndrome
disease > diseases of the osteoarticular system > skull disease > encephalocele > Meckel syndrome
... > disease > congenital disease > malformation > dysraphia > encephalocele > Meckel syndrome

Preferred term

Meckel syndrome  

Definition

  • 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)

Broader concept

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URI

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

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