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bn:03840398n
Noun Concept
SYL
No term available
EN
Meckel-Gruber syndrome is a rare, lethal ciliopathic genetic disorder, characterized by renal cystic dysplasia, central nervous system malformations, polydactyly, hepatic developmental defects, and pulmonary hypoplasia due to oligohydramnios. Wikipedia
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Sources
IS A
EN
rare disease
EN
dominance
EN
syndrome
EN
ciliopathy
HAS KIND
EN
Meckel syndrome type 7
EN
Grauhan syndrome
GENETIC ASSOCIATION
EN
MKS1
HEALTH SPECIALTY
EN
medical genetics
NAMED AFTER
EN
Johann Friedrich Meckel
EN
Georg Benno Gruber

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