Term Name:	Meckel syndrome 6
Synonyms:	Meckel-Gruber syndrome, type 6, MKS6
Definition:	A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32.
Ontology:	Human Disease [DOID:0070120]   ( DOID:0070120 )