L1CAM, L1 cell adhesion molecule, 3897

N. diseases: 289; N. variants: 35
Disease: Gait, Shuffling ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		0.400 Biomarker phenotype CTD_human MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. 7920660 1994
CUI: C0231688
Disease: Gait, Shuffling
Gait, Shuffling 		0.400 Biomarker phenotype HPO