Gene: NMNAT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64802
Gene Symbol: NMNAT1
NMNAT1 		0.410 Biomarker disease CTD_human Here we report that compound heterozygous and homozygous NMNAT1 mutations cause severe neonatal neurodegeneration of the central retina and early-onset optic atrophy in 22 unrelated individuals. 22842229 2012
Entrez Id: 64802
Gene Symbol: NMNAT1
NMNAT1 		0.410 GeneticVariation disease BEFREE Here we report that compound heterozygous and homozygous NMNAT1 mutations cause severe neonatal neurodegeneration of the central retina and early-onset optic atrophy in 22 unrelated individuals. 22842229 2012
Entrez Id: 64802
Gene Symbol: NMNAT1
NMNAT1 		0.410 Biomarker disease HPO