ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive
EDAR Causal
16435307 19438931 20979233 16029325 18231121 15373768 27657131 10431241
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive.
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Christ-siemens-touraine syndrome 1 shared geneEDAR Related via 1 shared gene including EDAR. Hypohidrotic ectodermal dysplasia 1 shared geneEDAR Related via 1 shared gene including EDAR. Mitochondrial dna depletion syndrome 1 shared geneEDAR Related via 1 shared gene including EDAR. Ectodermal dysplasia 1 shared geneEDAR Related via 1 shared gene including EDAR. Androgenetic alopecia 1 shared geneEDAR Related via 1 shared gene including EDAR.