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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
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Amyotrophic Lateral Sclerosis 1
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Rare Disease
Mosaic Genome-Wide Paternal Uniparental Disomy
Alias:
Genome-Wide Paternal Uniparental Disomy Mosaicism
Androgenetic/biparental Mosaicism
Mosaic Genome-Wide Paternal Upd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mosaic Genome-Wide Paternal Uniparental Disomy, also known as genome-wide paternal uniparental disomy mosaicism, is related to paternal uniparental disomy and beckwith-wiedemann syndrome. Affiliated tissues include placenta.
Related ID:
MALACARDS:MSC084
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
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Reference
MALACARDS
--
Antenatal
<1/1000000
--
--
--
MSC084
Medical Symptom
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Description
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Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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No data available
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Name
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No data available
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Category
Name
MGI
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