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X-linked intellectual disability-retinitis pigmentosa syndrome
MONDO:0010364
chromosome Xp21 deletion syndrome
MONDO:0010399
Xp22.3 microdeletion syndrome
MONDO:0015606
atypical Norrie disease due to monosomy Xp11.3
MONDO:0016850
partial deletion of the long arm of chromosome X
MONDO:0017007