Ectodermal dysplasia 13, hair/tooth type

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Subtype of: Ectodermal dysplasia
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Ectodermal dysplasia 13, hair/tooth type
MONDO_0016619
KREMEN1 Causal
27049303 29526031
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Ectodermal dysplasia 13, hair/tooth type.
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Ectodermal dysplasia 1 shared geneKREMEN1 Related via 1 shared gene including KREMEN1. Diverticular disease 1 shared geneKREMEN1 Related via 1 shared gene including KREMEN1. Uterine fibroid 1 shared geneKREMEN1 Related via 1 shared gene including KREMEN1. Androgenetic alopecia 1 shared geneKREMEN1 Related via 1 shared gene including KREMEN1. Kidney disease 1 shared geneKREMEN1 Related via 1 shared gene including KREMEN1.