Ectodermal Dysplasia and Immunodeficiency 2 (EDAID2)

Alias:

Edaid2

Ectodermal Dysplasia, Anhidrotic, with T-Cell Immunodeficiency, Autosomal Dominant

Ectodermal Dysplasia, Anhidrotic, with T-Cell Immunodeficiency Autosomal Dominant

Ectodermal Dysplasia, Hypohidrotic, with Immunodeficiency 2

Ectodermal Dysplasia, Hypohidrotic, with Immune Deficiency

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency 2

Ectodermal Dysplasia Hypohidrotic with Immunodeficiency

Dysplasia, Ectodermal, and Immunodeficiency, Type 2

Hed-Id

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Medical Symptom

Gene & Mutation

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References Literature

Ectodermal Dysplasia and Immunodeficiency 2, also known as edaid2, is related to ectodermal dysplasia and immune deficiency and ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive. An important gene associated with Ectodermal Dysplasia and Immunodeficiency 2 is NFKBIA (NFKB Inhibitor Alpha). Affiliated tissues include liver and lung, and related phenotypes are failure to thrive and splenomegaly

Related ID：

MALACARDS：ECT109

OMIM：612132

MESH：D004476