19p13.3 microduplication syndrome

Orpha code: 447980OMIM code:

Definition

A rare, genetic, syndromic intellectual disability characterized by intrauterine growth retardation, microcephaly, hypotonia, motor and neurodevelopmental delay, speech delay, intellectual disability, and mild dysmorphic features.

Disease data
Classification

Malformation syndrome

Synonyms
Dup(19)(p13.13)
Dup(19)(p13.13)
ORPHA code
447980
OMIM code
-
ICD10 code
Q92.3
ICD11 code
-

No additional description.

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