anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
This syndrome is characterized by severe immunodeficiency, osteopetrosis, lymphedema and anhidrotic ectodermal dysplasia
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anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
Summary
anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome is a developmental defect during embryogenesis[1].
Key Facts
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome's instance of is recorded as rare disease[3].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome's instance of is recorded as class of disease[4].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome is a type of syndrome with combined immunodeficiency[5].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome is a type of primary lymphedema with associated anomalies[6].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome is a type of syndromic lymphedema[7].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome is a type of genetic skin vascular disorder[8].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome's genetic association is recorded as IKBKG[9].
- anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_69088[10].