PRRX1, paired related homeobox 1, 5396

N. diseases: 134; N. variants: 11
Disease: Demyelination ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0011304
Disease: Demyelination
Demyelination 		phenotype Nervous System Diseases Pathologic Function 9 0.300 None 1.000 1 2018 2018