Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 259232
Gene Symbol: NALCN
NALCN
CUI: C0038379
Disease: Strabismus
Strabismus
0.100 CausalMutation CLINVAR A novel homozygous splice site mutation in NALCN identified in siblings with cachexia, strabismus, severe intellectual disability, epilepsy and abnormal respiratory rhythm. 26923739

2016

Entrez Id: 259232
Gene Symbol: NALCN
NALCN
CUI: C0038379
Disease: Strabismus
Strabismus
0.100 Biomarker HPO