STIL, STIL centriolar assembly protein, 6491

N. diseases: 88; N. variants: 9
Disease: Congenital, Hereditary, and Neonatal Diseases and Abnormalities ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027612
Disease: Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities 		0.010 GeneticVariation group LHGDN Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. 19215732 2009