Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type

MONDO:0015024

Any ectodermal dysplasia syndrome in which the cause of the disease is a mutation in the KDF1 gene.

Also known as: ECTD12, KDF1 ectodermal dysplasia syndrome, ectodermal dysplasia 12, hypohidrotic/hair/Tooth/nail type, ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type; ECTD12, ectodermal dysplasia syndrome caused by mutation in KDF1

0 clinical trials for this condition and its sub-types, 0 tagged with Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Ectodermal dysplasia syndrome (45)

Including sub-types (0) Tagged with Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.