Angelman Syndrome Due to Imprinting Defect in 15q11-Q13
Basic Information
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Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 is related to precocious puberty, central, 2 and schaaf-yang syndrome. An important gene associated with Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 is ATP10A (ATPase Phospholipid Transporting 10A (Putative)), and among its related pathways/superpathways is Prader-Willi and Angelman syndrome. Affiliated tissues include brain and skin, and related phenotypes are seizure and eeg abnormality
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Basic Information
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MALACARDS
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Infant
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3
29
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