Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84628
Gene Symbol: NTNG2
NTNG2
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.300 Biomarker GENOMICS_ENGLAND Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. 31668703

2019