SLC16A2, solute carrier family 16 member 2, 6567

N. diseases: 108; N. variants: 30
Disease: Neonatal Hypotonia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		0.110 GeneticVariation disease BEFREE A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay. 18166539 2008
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		0.110 Biomarker disease HPO