Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity
0.010 Biomarker disease BEFREE The condition is probably genetically heterogeneous, and other congenital insensitivity to pain and HSAN genes such as SCN11A may be implicated. 29949203 2018