ARX, aristaless related homeobox, 170302

N. diseases: 249; N. variants: 44
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.110 GeneticVariation phenotype BEFREE Severe congenital diarrhea occurs in approximately half of patients with Aristaless-Related Homeobox (ARX) null mutations.The cause of this diarrhea is unknown. 25171319 2015
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.110 Biomarker phenotype HPO