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MCID: CHR232
MIFTS: 10
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Chromosome 21, Uniparental Disomy
Categories:
Fetal diseases, Rare diseases
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MalaCards integrated aliases for Chromosome 21, Uniparental Disomy:
Name: Chromosome 21, Uniparental Disomy
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Classifications:External Ids:
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MalaCards based summary :
Chromosome 21, Uniparental Disomy, also known as chromosome 21, uniparental disomy of, is related to maternal uniparental disomy of chromosome 21 and paternal uniparental disomy of chromosome 21.
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Genetic tests related to Chromosome 21, Uniparental Disomy:
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Articles related to Chromosome 21, Uniparental Disomy:
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Search
GEO
for disease gene expression data for Chromosome 21, Uniparental Disomy.
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