Disease: Meningomyelocele ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.110 Biomarker disease BEFREE PCP rare putative mutations had a weaker role in myelomeningocele (SB), being found in approximately 6% of cases and cumulated across CELSR1, FUZ, FZD6, PRICKLE1, VANGL1, and VANGL2. 23024041 2012
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.110 Biomarker disease HPO