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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Chromosomal disorder
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Syndrome caused by partial chromosomal deletion
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Partial deletion of chromosome 12
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Chromosome 12p deletion
12p12.1 microdeletion syndrome
rare
Identifiers
MONDO:0017781
Orphanet:313884
Part of
Chromosome 12p deletion
Also known as
Del(12)(p12.1) · monosomy 12p12.1
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