Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 93587
Gene Symbol: TRMT10A
TRMT10A
CUI: C0431350
Disease: Primary microcephaly
Primary microcephaly
0.310 Biomarker GENOMICS_ENGLAND Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities. 26535115

2015