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20p12.3 microdeletion syndrome

Disease Export to PDF
Name:
20p12.3 microdeletion syndrome
Description:
20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome (see this term), variable developmental delay and facial dysmorphism.
ORPHAcode:
261295
Synonyms:
Del(20)(p12.3)
Monosomy 20p12.3
XREF(s):
Orphanet
ICD-10
Analyte(s):
BMP2
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14