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Results 1 - 8 of 8 for eda
  1. EDA gene 
    The EDA gene provides instructions for making a protein called ectodysplasin A. This protein is part of a signaling pathway that plays an important role ...
    https://medlineplus.gov/genetics/gene/eda - Genetics
  2. Anhidrotic ectodermal dysplasia with immune deficiency 
    Anhidrotic ectodermal dysplasia with immune deficiency (EDA-ID) is a form of ectodermal dysplasia, which is a group of conditions characterized by abnormal development of ectodermal tissues including the ...
    https://medlineplus.gov/...todermal-dysplasia-with-immune-deficiency - Genetics
  3. IKBKG gene 
    ... to cause anhidrotic ectodermal dysplasia with immune deficiency (EDA-ID). EDA-ID is a condition characterized by abnormal development ... immune system function is reduced in people with EDA-ID, resulting in recurrent infections.The IKBKG gene ...
    https://medlineplus.gov/genetics/gene/ikbkg - Genetics
  4. EDAR gene 
    ... a protein called ectodysplasin A1 (produced from the EDA gene). On the cell surface, ectodysplasin A1 attaches ... A1 isoform receptor ectodysplasin receptor ED1R ED3 ED5 EDA-A1R EDA1R EDA3 EDAR_HUMAN Tests of EDAR ...
    https://medlineplus.gov/genetics/gene/edar - Genetics
  5. Hypohidrotic ectodermal dysplasia 
    ... mutations in one of several genes. These include EDA, EDAR, EDARADD, and WNT10A. EDA gene mutations are the most common cause of ... ectodermal dysplasia, the genetic cause is unknown.The EDA, EDAR, and EDARADD genes provide instructions for making ...
    https://medlineplus.gov/.../hypohidrotic-ectodermal-dysplasia - Genetics
  6. NFKBIA gene 
    ... to cause anhidrotic ectodermal dysplasia with immune deficiency (EDA-ID). EDA-ID is a condition characterized by reduced function ... ectodermal tissues. The NFKBIA gene mutations that cause EDA-ID impair the protein's breakdown. As a ...
    https://medlineplus.gov/genetics/gene/nfkbia - Genetics
  7. What is Prader-Willi Syndrome? (Prader-Willi Syndrome Association)  
    Prader-Willi Syndrome/Learn More ... Prader-Willi Syndrome ... Prader-Willi Syndrome (PWS) is a rare genetic disorder characterized by chronic hunger, growth hormone ...
    https://www.pwsausa.org/what-is-prader-willi-syndrome - External Health Links
  8. Clinical Trial Diversity (Food and Drug Administration)  
    Health Disparities/Statistics and Research ... Health Disparities ... Clinical Trials/Related Issues ... Clinical Trials ... Food and Drug Administration ... People from racial ...
    https://www.fda.gov/.../clinical-trial-diversity - External Health Links