A cytogenetic abnormality that refers to the allelic loss of all or part of the long arm of chromosome 13.
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Smith-Magenis syndrome
MONDO:0008434
severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
MONDO:0010334
distal monosomy 13q
MONDO:0011248
chromosome 13q14 deletion syndrome
MONDO:0013481
partial chromosome Y deletion
MONDO:0015607
partial deletion of chromosome 1
MONDO:0016866