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Collaborative Research
Diseases
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Disorder of development or morphogenesis
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Hypohidrotic ectodermal dysplasia
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Autosomal dominant hypohidrotic ectodermal dysplasia
Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant
rare
Identifiers
MONDO:0013982
OMIM:614940
Causal genes
EDARADD
Part of
Autosomal dominant hypohidrotic ectodermal dysplasia
Also known as
ECTD11A
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