Term Name:	Meckel syndrome 7
Synonyms:	Meckel-Gruber syndrome, type 7, MKS7
Definition:	A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the NPHP3 gene on chromosome 3q22.1.
Ontology:	Human Disease [DOID:0070121]   ( DOID:0070121 )