TCTN2, tectonic family member 2, 79867

N. diseases: 109; N. variants: 15
Disease: POLYDACTYLY, POSTAXIAL ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		0.300 Biomarker disease GENOMICS_ENGLAND A TCTN2 mutation defines a novel Meckel Gruber syndrome locus. 21462283 2011