Anhidrotic Ectodermal Dysplasia 1

An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN.

Also Known As:

Ectodermal Dysplasia 1, Anhidrotic; Anhidrotic Ectodermal Dysplasia, X-Linked; Anhydrotic Ectodermal Dysplasia, X-Linked; CST Syndrome; Ectodermal Dysplasia 1; Ectodermal Dysplasia 1, Anhydrotic; Ectodermal Dysplasia, Anhidrotic, X-Linked; Ectodermal Dysplasia, Hypohidrotic, X-Linked; Ectodermal Dysplasia, Hypohydridic, X-Linked; Hypohidrotic Ectodermal Dysplasia; X-Linked Hypohydridic Ectodermal Dysplasia; Anhidrotic Ectodermal Dysplasia, X Linked; Anhydrotic Ectodermal Dysplasia, X Linked; CST Syndromes; Christ Siemens Touraine Syndrome; Dysplasia 1, Ectodermal; Ectodermal Dysplasia 1s; Syndrome, CST; Syndromes, CST; X Linked Hypohydridic Ectodermal Dysplasia; Christ-Siemens-Touraine Syndrome

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Multiple Abnormalities: 213
    - Ectodermal Dysplasia: 512
      - Anhidrotic Ectodermal Dysplasia 1: 161
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 512
      - Anhidrotic Ectodermal Dysplasia 1: 161
- Inborn Genetic Diseases: 12342
  - Genetic Skin Diseases: 51
    - Ectodermal Dysplasia: 512
      - Anhidrotic Ectodermal Dysplasia 1: 161
  - X-Linked Genetic Diseases: 42
    - Anhidrotic Ectodermal Dysplasia 1: 161
Skin and Connective Tissue Diseases
- Skin Diseases: 13402
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 512
      - Anhidrotic Ectodermal Dysplasia 1: 161
  - Genetic Skin Diseases: 51
    - Ectodermal Dysplasia: 512
      - Anhidrotic Ectodermal Dysplasia 1: 161

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M O Lexner Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure