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MCID: PTR021
MIFTS: 4
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Paternal Uniparental Disomy of Chromosome 21
Categories:
Fetal diseases, Rare diseases
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MalaCards integrated aliases for Paternal Uniparental Disomy of Chromosome 21:
Name: Paternal Uniparental Disomy of Chromosome 21
58
Classifications:
ICD10:
33
Orphanet: 58
Developmental anomalies during embryogenesis External Ids:
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MalaCards based summary :
Paternal Uniparental Disomy of Chromosome 21, is also known as upd(21)pat.
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Search
GEO
for disease gene expression data for Paternal Uniparental Disomy of Chromosome 21.
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