Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10653
Gene Symbol: SPINT2
SPINT2
CUI: C0152426
Disease: Craniorachischisis
Craniorachischisis 		0.300 Biomarker CTD_human Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea. 24722141

2014