Meckel syndrome (Q1915681)

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a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia.
  • Meckel-Gruber syndrome
  • Meckel–Gruber Syndrome
  • Gruber Syndrome
  • Dysencephalia Splanchnocystica
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English
Meckel syndrome
a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia.
  • Meckel-Gruber syndrome
  • Meckel–Gruber Syndrome
  • Gruber Syndrome
  • Dysencephalia Splanchnocystica

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