Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive
0.100 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980

2015