Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
0.100 Biomarker phenotype HPO
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
0.100 GeneticVariation phenotype CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015