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Summary Literature (0)
DOID:0070122 - Meckel syndrome 8

Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TCTN2 gene on chromosome 12q24.31.

Synonyms: Meckel-Gruber syndrome, type 8, MKS8

Xenbase Genes : tctn2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013482 - Meckel syndrome, type 8

MIM:
MIM:613885 - MECKEL SYNDROME, TYPE 8; MKS8

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)