Gene: NKX6-2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84504
Gene Symbol: NKX6-2
NKX6-2 		0.110 GeneticVariation disease BEFREE NKX6-2 mutations should be considered in patients with autosomal recessive, very early onset of nystagmus, cerebellar ataxia with hypotonia that rapidly progresses to spasticity, particularly when associated with neuroimaging signs of hypomyelination. 31509304 2020
Entrez Id: 84504
Gene Symbol: NKX6-2
NKX6-2 		0.110 Biomarker disease HPO