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Concept information

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

Terme préférentiel

Meckel syndrome  

Définition

  • 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)

Concept générique

Traductions

URI

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

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