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Echinobase
Summary Literature (0)
DOID:0070117 - Meckel syndrome 3

Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM67 gene on chromosome 8q22.1.

Synonyms: Meckel-Gruber syndrome, type 3, MKS3

Echinobase Genes : tmem67


MIM:
MIM:607361 - meckel syndrome, type 3; mks3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Meckel syndrome (is_a)