Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 91147
Gene Symbol: TMEM67
TMEM67
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies
0.100 CausalMutation CLINVAR Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). 19508969

2009

Entrez Id: 91147
Gene Symbol: TMEM67
TMEM67
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies
0.100 GeneticVariation CLINVAR