Epilepsy with auditory features

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
AUTOSOMAL DOMINANT EPILEPSY WITH AUDITORY FEATURES
MONDO:0010898
LGI1 Causal
11810107 11978770 14510822 15009222 15079011 16787412 16990550 17296837 20130004 20133599 20659151 20659958 22496201 24206907 25485908 26773249
ClinGen, GWAS catalog
DEPDC5 Unknown
23542697 23542701
GWAS catalog
RELN Unknown
26046367
ClinVar
EPILEPSY WITH AUDITORY FEATURES
101046
LGI1 Unknown
12601709 20301709
Orphanet
MICAL1 Unknown
29394500
Orphanet
RELN Unknown
26046367
Orphanet
All4 Causal1 Unknown4
Related Diseases Diseases that share the most curated genes with Epilepsy with auditory features.
5 View disease cluster →
Lateral temporal lobe epilepsy 3 shared genesRELN, DEPDC5, LGI1 Related via 3 shared genes including RELN, DEPDC5, LGI1. Familial temporal lobe epilepsy 3 shared genesRELN, LGI1, MICAL1 Related via 3 shared genes including RELN, LGI1, MICAL1. Sacroiliac arthritis 1 shared geneRELN Related via 1 shared gene including RELN. Sacroiliac joint synovitis 1 shared geneRELN Related via 1 shared gene including RELN. lissencephaly with cerebellar hypoplasia 1 shared geneRELN Related via 1 shared gene including RELN.