Orphanet classification of chromosomal anomalies sorted by chromosome
- Rare chromosomal anomaly
ORPHA:68335 -
Autosomal anomaly
ORPHA:98127 -
Anomaly of chromosome 11
ORPHA:261730 -
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion ORPHA:231130
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Partial deletion of chromosome 11 ORPHA:261816
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Partial duplication of chromosome 11 ORPHA:262653
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Ring chromosome 11 syndrome ORPHA:96175
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Uniparental disomy of chromosome 11 ORPHA:263034
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