Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		0.200 Biomarker MGD

Entrez Id: 162
Gene Symbol: AP1B1
AP1B1
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		0.200 Biomarker MGD