Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4784
Gene Symbol: NFIX
NFIX
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
0.110 GeneticVariation BEFREE Microdeletions and loss of function variants of NFIX are responsible for Sotos syndrome-2 (also described as Malan syndrome), a syndromic form of intellectual disability associated with overgrowth and macrocephaly. 29184170

2018

Entrez Id: 4784
Gene Symbol: NFIX
NFIX
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
0.110 Biomarker HPO