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  2. 1p21.3 microdeletion syndrome

1p21.3 microdeletion syndrome

Disease Export to PDF
Name:
1p21.3 microdeletion syndrome
Description:
1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder(see this term).
ORPHAcode:
293948
Synonyms:
Del(1)(p21.3)
Monosomy 1p21.3
XREF(s):
Orphanet
ICD-10
Analyte(s):
DPYD
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14