Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2303
Gene Symbol: FOXC2
FOXC2
CUI: C0033377
Disease: Ptosis
Ptosis
0.110 GeneticVariation BEFREE Here we describe a case of LD carrying a de novo frameshift mutation of FOXC2 who presented a prepubertal onset of lower limbs lymphedema and mild distichiasis associated with other anomalies such as webbing neck and ptosis. 20450314

2010

Entrez Id: 2303
Gene Symbol: FOXC2
FOXC2
CUI: C0033377
Disease: Ptosis
Ptosis
0.110 Biomarker HPO