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Mowat-Wilson syndrome due to monosomy 2q22

rare
Identifiers
MONDO:0016855 Orphanet:261537
Part of
Mowat-Wilson syndromePartial deletion of the long arm of chromosome 2
Also known as
Hirschsprung disease and intellectual disability due to 2q22 microdeletion · Hirschsprung disease and intellectual disability due to del(2)(q22) · Hirschsprung disease and intellectual disability due to monosomy 2q22 · Mowat-Wilson syndrome due to 2q22 microdeletion · Mowat-Wilson syndrome due to del(2)q(22)

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