Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 497231
Gene Symbol: CLN9
CLN9
0.020 Biomarker disease BEFREE A new variant of a group of pediatric neurodegenerative diseases known as neuronal ceroid lipofuscinosis (NCL) or Batten disease has been identified.It is termed CLN9-deficient. 16303764 2006
Entrez Id: 497231
Gene Symbol: CLN9
CLN9
0.020 GeneticVariation disease BEFREE We describe the ninth variant of neuronal ceroid lipofuscinosis (NCL) or Batten disease, due to defects in a putative new gene, CLN9. 15349861 2004
Entrez Id: 497231
Gene Symbol: CLN9
CLN9
0.020 GeneticVariation disease LHGDN We describe the ninth variant of neuronal ceroid lipofuscinosis (NCL) or Batten disease, due to defects in a putative new gene, CLN9. 15349861 2004