TMEM98, transmembrane protein 98, 26022

N. diseases: 22; N. variants: 3
Disease: Retinal defect ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0154823
Disease: Retinal defect
Retinal defect 		0.010 Biomarker phenotype BEFREE Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse. 31266059 2019