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ENCranioectodermal Dysplasia 3 (CED3)
Alias:
Ced3
Dysplasia, Cranioectodermal, Type 3
Sensenbrenner Syndrome 3
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Cranioectodermal Dysplasia 3, is also known as ced3, and has symptoms including dry skin An important gene associated with Cranioectodermal Dysplasia 3 is IFT43 (Intraflagellar Transport 43). Affiliated tissues include skin and heart, and related phenotypes are dolichocephaly and widely spaced teeth
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