NOG, noggin, 9241

N. diseases: 206; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
0.110 GeneticVariation disease BEFREE We conclude that p.G92E represents a rare polymorphism of the NOGGIN gene-- causing neither brachydactyly nor fibrodysplasia ossificans progressiva. 22529972 2012
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
0.110 Biomarker disease HPO