Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005686
Disease: Urinary Bladder Diseases
Urinary Bladder Diseases
0.320 GeneticVariation group BEFREE This is the first independent report of biallelic variants in CHRM3 in a family with a rare serious bladder disorder associated with mydriasis and provides important evidence of this association. 31441039 2019
CUI: C0005686
Disease: Urinary Bladder Diseases
Urinary Bladder Diseases
0.320 GeneticVariation group BEFREE Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. 22077972 2011
CUI: C0005686
Disease: Urinary Bladder Diseases
Urinary Bladder Diseases
0.320 Biomarker group CTD_human Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome. 22077972 2011