Human genes for Meckel syndrome 3
Meckel syndrome 3 [DOID:0070117]
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TMEM67 on chromosome 8q22.1.
Synonyms: Meckel syndrome 3, DOID:0070117, Meckel-Gruber syndrome, type 3, MKS3, MeckelGruber syndrome type 3 ...