2p15-16.1 microdeletion syndrome
2p15-16.1 microdeletion is an extremely rare genetic disorder caused by a small deletion in the short arm of human chromosome 2. First described in two patients in 2007, by 2013 only 21 people have been reported as having the disorder in the medical literature.
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2p15-16.1 microdeletion syndrome
2p15-16.1 microdeletion is an extremely rare genetic disorder caused by a small deletion in the short arm of human chromosome 2. First described in two patients in 2007, by 2013 only 21 people have been reported as having the disorder in the medical literature.
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2p15-16.1 microdeletion is an ...... der in the medical literature.
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17,350,393
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1,017,833,512
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Chromosome 2
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ICD
Q93.5
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OMIM
Orphanet
synonyms
Monosomy 2p15-p16.1
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2p15-16.1 microdeletion is an ...... der in the medical literature.
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2p15-16.1 microdeletion syndrome
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