FEZF1, FEZ family zinc finger 1, 389549

N. diseases: 73; N. variants: 3
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4014988
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA 		0.600 GeneticVariation disease UNIPROT Mutations in FEZF1 cause Kallmann syndrome. 25192046 2014
CUI: C4014988
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in FEZF1 cause Kallmann syndrome. 25192046 2014
CUI: C4014988
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in FEZF1 cause Kallmann syndrome. 25192046 2014
CUI: C4014988
Disease: HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA 		0.600 Biomarker disease CTD_human