/Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15

Rare Disease

MONDO:0020298

Also Known As

Prader-Willi syndrome due to maternal uniparental disomy of chromosome type 15UPD(15)mat

Comprehensive, easy-to-understand information about this condition

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Schaaf-Yang syndrome

MONDO:0014243

mosaic trisomy 15

MONDO:0015727

Prader-Willi syndrome due to translocation

MONDO:0015785

Prader-Willi syndrome due to imprinting mutation

MONDO:0015786

ring chromosome 15

MONDO:0019908

Prader-Willi syndrome due to paternal 15q11q13 deletion

MONDO:0020301