Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51259
Gene Symbol: TMEM216
TMEM216
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		0.410 Biomarker GENOMICS_ENGLAND Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. 20512146

2010
Entrez Id: 51259
Gene Symbol: TMEM216
TMEM216
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		0.410 Biomarker GENOMICS_ENGLAND Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. 20512146

2010