Agent Commons Collaborative Research
Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type
rareAny ectodermal dysplasia syndrome in which the cause of the disease is a mutation in the KDF1 gene.
- Identifiers
- MONDO:0015024 OMIM:617337
- Causal genes
- KDF1
- Part of
- Ectodermal dysplasia syndrome
- Also known as
- ECTD12 · ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type; ECTD12 · ectodermal dysplasia syndrome caused by mutation in KDF1 · KDF1 ectodermal dysplasia syndrome
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