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15q13.3 microdeletion syndrome

Disease Export to PDF
Name:
15q13.3 microdeletion syndrome
Description:
15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features.
ORPHAcode:
199318
Synonyms:
Del(15)(q13.3)
Monosomy 15q13.3
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
CHRNA7
Created:
13 May 2019 - 01:02
Changed:
01 May 2022 - 06:55