Epidermodysplasia verruciformis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
EPIDERMODYSPLASIA VERRUCIFORMIS
MESH:D004819MONDO:0009176
TMC6 Causal
30036492
CTD
TMC8 Causal
12426567
GWAS catalog —
CIB1 Unknown
30068544
GWAS catalog —
CORO1A Unknown — GenCC
IL7 Unknown
25981006
GWAS catalog
MST1 Unknown — GenCC
RHOH Unknown — GenCC
EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 1
MONDO:0100045
TMC6 Causal
12426567 17011789
CTD, ClinVar
EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 2
MONDO:0032614
TMC8 Causal
12426567 17011789
ClinVar, GWAS catalog —
EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3
MONDO:0032644
CIB1 Causal
34386043
ClinVar, Disgenet —
EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 4
MONDO:0032666
RHOH Unknown
22850876
ClinGen, ClinVar, GWAS catalog
EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 5
MONDO:0032667
IL7 Causal
25981006
ClinVar, GWAS catalog
All7 Causal4 Unknown5
Related Diseases Diseases that share the most curated genes with Epidermodysplasia verruciformis.
5 View disease cluster →
severe combined immunodeficiency due to CORO1A deficiency 1 shared geneCORO1A Related via 1 shared gene including CORO1A. Thyroid gland neoplasms 1 shared geneRHOH Related via 1 shared gene including RHOH. Cholangitis 1 shared geneMST1 Related via 1 shared gene including MST1. Immunodeficiency 4 shared genesRHOH, CORO1A, MST1, IL7 Related via 4 shared genes including RHOH, CORO1A, MST1. Combined immunodeficiency disease 1 shared geneMST1 Related via 1 shared gene including MST1.