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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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Uniparental disomy
Maternal uniparental disomy of chromosome 21
rare
Identifiers
MONDO:0019918
Orphanet:96187
Part of
Chromosome 21 disorder
Uniparental disomy
Also known as
maternal uniparental disomy of chromosome type 21 · UPD(21)mat
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