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Diseases / Disorder of development or morphogenesis/ Developmental defect during embryogenesis/ Multiple congenital anomalies/dysmorphic syndrome/ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability/ Chromosome 19q13.11 deletion syndrome

Chromosome 19q13.11 deletion syndrome, proximal

rare

Chromosome 19q13.11 deletion syndrome in which the proximal region was deleted.

Identifiers: MONDO:0014972 OMIM:617219
Part of: Chromosome 19q13.11 deletion syndrome

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