WNT1, Wnt family member 1, 7471

N. diseases: 216; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia
0.110 GeneticVariation disease BEFREE A murine model resembling this dysgenesis is demonstrated by homozygous mutations of the organizer genes Wnt1 or En1, also resulting in cerebellar aplasia, and En2, associated with cerebellar hypoplasia. 11815869 2002
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia
0.110 Biomarker disease HPO