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Results: 2

1.

Meckel syndrome type 1

MedGen UID:
811346
Concept ID:
C3714506
Disease or Syndrome
2.

Meckel-Gruber syndrome

A rare, lethal, autosomal recessive inherited syndrome characterized by pulmonary hypoplasia, central nervous system malformations, and hepatic malformations. [from NCI]

MedGen UID:
120513
Concept ID:
C0265215
Disease or Syndrome

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