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Diseases / Disease of genetic or genomic mechanism/ Chromosomal disorder/ Syndrome caused by partial chromosomal deletion/ Partial deletion of the long arm of chromosome 21

21q22.11q22.12 microdeletion syndrome

rare

Identifiers: MONDO:0016845 Orphanet:261323
Part of: Partial deletion of the long arm of chromosome 21
Also known as: 21q22.11-q22.12 microdeletion syndrome · Del(21)(q22.11q22.12) · monosomy 21q22.11-q22.12 · monosomy 21q22.11q22.12

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