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GTR Home > Conditions/Phenotypes > Meckel-Gruber syndrome

Summary

A rare, lethal, genetic, multiple congenital anomaly disorder characterized by the triad of brain malformation (mainly occipital encephalocele), large polycystic kidneys, and polydactyly, as well as associated abnormalities that may include cleft lip/palate, cardiac and genital anomalies, central nervous system (CNS) malformations, liver fibrosis, and bone dysplasia. [from ORDO]

Genes See tests for all associated and related genes

  • Related genesHelp

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