Enlarged vestibular aqueduct

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Enlarged vestibular aqueduct
HP:0011387
FOXI1 Unknown
29242249 9843211 16932748 41833579 15173882 8825632 7957066 12642503 17503324
Open Targets —
SLC26A4 Unknown
10190331 10192399 10404839 10449762 10571950 10602116 10843192 10861298 10878664 10902795 11152663 11274445 11317356 11932316 12107249 12354788 12642503 12676893 12727986 12788906 12920581 12974744 14508505 15531480 15679828 15689455 16260629 16570074 17443271 17503324 17690912 17718863 17940114 18285825 18310264 19204907 19287372 19426954 20442411 22139968 8541853 9302427 9398842 9500541 9618166 9618167 9729124 9920104
Open Targets
Enlarged vestibular aqueduct, digenic
MONDO_0010933
KCNJ10 Unknown
22328087 19426954 20807765 10856114 11466414 17942730 21849804 19289823 7608203 9367690 19420365 20651251 7580148 12618319
Open Targets
Enlarged vestibular aqueducts0
MONDO_0010933
FOXI1 Unknown
29242249
Open Targets —
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Enlarged vestibular aqueduct.
5 View disease cluster →
Pendred syndrome 3 shared genesSLC26A4, FOXI1, KCNJ10 Related via 3 shared genes including SLC26A4, FOXI1, KCNJ10. Mondini defect 1 shared geneSLC26A4 Related via 1 shared gene including SLC26A4. Deafness, autosomal recessive 4, with enlarged vestibular aqueduct 1 shared geneSLC26A4 Related via 1 shared gene including SLC26A4. Deafness, autosomal recessive, 4 1 shared geneSLC26A4 Related via 1 shared gene including SLC26A4. East syndrome 1 shared geneKCNJ10 Related via 1 shared gene including KCNJ10.