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DOID:0070122 - Meckel syndrome 8
Disease Ontology Definition:A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of TCTN2 on chromosome 12q24.31.
Synonyms: MKS8, Meckel-Gruber syndrome, type 8,
Echinobase Genes :
MIM:613885 - meckel syndrome, type 8; mks8 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Meckel syndrome (is_a)