Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56652
Gene Symbol: TWNK
TWNK
CUI: C0033377
Disease: Ptosis
Ptosis
0.110 GeneticVariation BEFREE Autosomal dominant progressive external ophthalmoplegia due to the p.R357P PEO1 mutation is a late-onset ocular myopathy beginning with ptosis and progressing slowly. 24018892

2013

Entrez Id: 56652
Gene Symbol: TWNK
TWNK
CUI: C0033377
Disease: Ptosis
Ptosis
0.110 Biomarker HPO