MAP7, microtubule associated protein 7, 9053

N. diseases: 10; N. variants: 0
Disease: Sacral dysgenesis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0431414
Disease: Sacral dysgenesis
Sacral dysgenesis 		0.010 Biomarker disease BEFREE We then evaluated the involvement of MAP7 in SD by further screening of the gene in several patients with a similar phenotype. 15218243 2004