Sensorineural deafness

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
sensorineural deafness
MONDO_0020678
GLIS3 Unknown
16715098 26259131
Open Targets —
LHX3 Unknown
10835633 21249393 18407919 26416826
Open Targets —
SLC26A4 Unknown
11932316 9398842
Open Targets
All3 Causal0 Unknown3
Related Diseases Diseases that share the most curated genes with Sensorineural deafness.
5 View disease cluster →
Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidney syndrome 1 shared geneGLIS3 Related via 1 shared gene including GLIS3. 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. Winkelman bethge pfeiffer syndrome 1 shared geneLHX3 Related via 1 shared gene including LHX3.