19p13.3 microduplication syndrome

Disease Export to PDF
Name:
19p13.3 microduplication syndrome
Description:
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.
ORPHAcode:
447980
Synonyms:
Dup(19)(p13.13)
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14