Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0070116 - Meckel syndrome 2

Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM216 gene on chromosome 11q12.2.

Synonyms: Meckel-Gruber syndrome, type 2, MKS2

Xenbase Genes : tmem216

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011296 - Meckel syndrome, type 2


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)