Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25794
Gene Symbol: FSCN2
FSCN2
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.320 GeneticVariation LHGDN Experiments were performed to investigate the gene and allele copy numbers of FSCN2 in patients with RP who have the c.72delG mutation as well as healthy subjects with or without the mutation. 18450588

2008
Entrez Id: 25794
Gene Symbol: FSCN2
FSCN2
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.320 GeneticVariation LHGDN Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene. 14609921

2003