Source: MGD

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C0265242
Disease: Otocephaly
Otocephaly 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		disease 0.200 None 0 0
Entrez Id: 8928
Gene Symbol: FOXH1
FOXH1 		forkhead box H1 0.615 0.654 4.2E-02
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		disease 0.200 None 0 0