NELL1, neural EGFL like 1, 4745

N. diseases: 122; N. variants: 23
Disease: Congenital premature fusion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332877
Disease: Congenital premature fusion
Congenital premature fusion 		0.010 AlteredExpression disease BEFREE In conclusion, our data suggest that the NELL-1 gene is preferentially expressed in cranial intramembranous bone and neural tissue (both of neural crest cell origin) and is up-regulated during unilateral premature closure of the coronal suture. 9893069 1999