Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		0.370 Biomarker GENOMICS_ENGLAND Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4. 11567216

2001
Entrez Id: 89884
Gene Symbol: LHX4
LHX4
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		0.370 Biomarker GENOMICS_ENGLAND Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4. 11567216

2001
Entrez Id: 3170
Gene Symbol: FOXA2
FOXA2
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		0.320 Biomarker GENOMICS_ENGLAND Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities. 28973288

2017
Entrez Id: 5617
Gene Symbol: PRL
PRL
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		0.310 Biomarker CTD_human [Importance of prolactin level indication in detection of Sheehan syndrome]. 1304515

1992
Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		0.300 Biomarker CTD_human Congenital hypopituitarism as a cause of undetectable estriol levels in the maternal triple-marker screen. 12970278

2003
Entrez Id: 1586
Gene Symbol: CYP17A1
CYP17A1
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		0.300 Biomarker CTD_human Congenital hypopituitarism as a cause of undetectable estriol levels in the maternal triple-marker screen. 12970278

2003