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Causes of Ectodermal dysplasia, hypohidrotic, autosomal dominant

Causes of Ectodermal dysplasia, hypohidrotic, autosomal dominant

Ectodermal dysplasia, hypohidrotic, autosomal dominant is caused by a mutation in the EDAR gene (ectodysplasin anhidrotic receptor) or the EDARADD gene (EDAR-associated death domain).

Ectodermal dysplasia, hypohidrotic, autosomal dominant: Related Medical Conditions

To research the causes of Ectodermal dysplasia, hypohidrotic, autosomal dominant, consider researching the causes of these these diseases that may be similar, or associated with Ectodermal dysplasia, hypohidrotic, autosomal dominant:

Ectodermal dysplasia, hypohidrotic, autosomal dominant: Causes and Types

Causes of Broader Categories of Ectodermal dysplasia, hypohidrotic, autosomal dominant: Review the causal information about the various more general categories of medical conditions:

Related information on causes of Ectodermal dysplasia, hypohidrotic, autosomal dominant:

As with all medical conditions, there may be many causal factors. Further relevant information on causes of Ectodermal dysplasia, hypohidrotic, autosomal dominant may be found in:

 

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