FEZF1, FEZ family zinc finger 1, 389549

N. diseases: 73; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
0.310 GermlineCausalMutation disease ORPHANET Mutations in FEZF1 cause Kallmann syndrome. 25192046 2014
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
0.310 GeneticVariation disease BEFREE Mutations in FEZF1 cause Kallmann syndrome. 25192046 2014