LSS, lanosterol synthase, 4047

N. diseases: 74; N. variants: 10
Disease: Microcephaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.300 Biomarker disease GENOMICS_ENGLAND Congenital cataract with LSS gene mutations: a new case report. 29016354 2017