RS121908116 EDARADD
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What This Variant Does
"[OMIM:?]
Associated Conditions
Ectodermal dysplasia 11A
hypohidrotic/hair/tooth type
autosomal dominant
Ectodermal dysplasia 10A
hypohidrotic/hair/nail type
Ectodermal dysplasia 11A
hypohidrotic/hair/tooth type
autosomal dominant
Ectodermal dysplasia 10A
hypohidrotic/hair/nail type
Other Variants in EDARADD