Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
HETEROTAXY SYNDROME	C3178805 MESH:D059446	ACVR2B	Unknown	9916847	CTD Disgenet
		CERS1	Unknown	—	Disgenet
		CFAP52	Unknown	—	Disgenet
		CFC1B	Unknown	—	Disgenet
		CIROZ	Unknown	—	Disgenet
		CRIPTO	Unknown	11062482	CTD Disgenet
		DAW1	Unknown	—	Disgenet
		FOXP1	Unknown	—	Disgenet
		GDF1	Unknown	—	CTD Disgenet
		LEFTY2	Unknown	10053005	CTD Disgenet
		MMP21	Unknown	26437028	CTD Disgenet
		PKD1L1	Unknown	—	Disgenet
HETEROTAXY, VISCERAL, 1, X-LINKED	306955 C1844020 MONDO:0010607	ZIC3	Causal	—	ClinVar Disgenet GenCC HPO
HETEROTAXY, VISCERAL, 10, AUTOSOMAL, WITH MALE INFERTILITY	619607 C5562072 MONDO:0030474	CFAP52	Causal	—	ClinVar Disgenet HPO
HETEROTAXY, VISCERAL, 11, AUTOSOMAL, WITH MALE INFERTILITY	619608 C5562019 MONDO:0030475	CFAP45	Causal	—	ClinVar Disgenet GenCC HPO
HETEROTAXY, VISCERAL, 12, AUTOSOMAL	619702 C5676898 MONDO:0859222	CIROP	Causal	—	ClinVar Disgenet HPO
HETEROTAXY, VISCERAL, 13, AUTOSOMAL	621079 MONDO:0976134	DAND5	Unknown	—	ClinVar HPO
HETEROTAXY, VISCERAL, 14, AUTOSOMAL	621080 MONDO:0976135	CIROZ	Unknown	—	ClinVar HPO
HETEROTAXY, VISCERAL, 2, AUTOSOMAL	605376 C1415817 MONDO:0011546 OMIM:605376	CFC1	Causal	11062482 17072672 18538293 21864452 25423076	CTD ClinVar Disgenet HPO Orphanet
HETEROTAXY, VISCERAL, 4, AUTOSOMAL	613751 C3151057 MONDO:0013403 OMIM:613751	ACVR2B	Causal	21864452 30029678 30120289 30622330 9916847	CTD ClinVar Disgenet GWAS catalog HPO
HETEROTAXY, VISCERAL, 4, AUTOSOMAL	613751 C3151057 MONDO:0013403 OMIM:613751	PIEZO2	Causal	—	Disgenet
HETEROTAXY, VISCERAL, 5, AUTOSOMAL	270100 MONDO:0700112 OMIM:270100	NODAL	Causal	—	CTD ClinVar GenCC HPO
HETEROTAXY, VISCERAL, 6, AUTOSOMAL	614779 C3553676 MONDO:0013887 OMIM:614779	CFAP53	Causal	22577226 25504577 26531781	CTD ClinVar Disgenet HPO
HETEROTAXY, VISCERAL, 7, AUTOSOMAL	616749 C4225217 MONDO:0014762 OMIM:616749	MMP21	Causal	26437029 26437028 26429889	CTD ClinVar Disgenet HPO
HETEROTAXY, VISCERAL, 8, AUTOSOMAL	617205 C4310668 MONDO:0014967 OMIM:617205	PKD1L1	Causal	27616478 35691949	CTD ClinVar Disgenet HPO
HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY	618948 C5394551 MONDO:0030070	MNS1	Causal	22396656 30148830 31534215	ClinVar Disgenet HPO
HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY	618948 C5394551 MONDO:0030070	TEX9	Unknown	—	Disgenet
HETEROTAXY, VISCERAL, X-LINKED	MESH:C538116	ZIC3	Unknown	—	CTD

Heterotaxy syndrome