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EN20p13 Microdeletion Syndrome
Alias:
20p Subtelomeric Deletion Syndrome
Monosomy 20p13
Del(20)(p13)
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20p13 Microdeletion Syndrome, also known as 20p subtelomeric deletion syndrome, is related to hydrocephalus, congenital, 1 and absence of septum pellucidum. Affiliated tissues include eye, and related phenotypes are motor delay and intellectual disability
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Basic Information
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MALACARDS
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