Coffin-Siris syndrome 6
MONDO:0033492Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID2 gene.
Also known as: ARID2-related BAFopathy, Coffin-Siris syndrome 6, COFFIN-SIRIS syndrome 6, CSS6
0 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Nervous system disorder
(231)
Hereditary disease
(176)
Neurodevelopmental disorder
(147)
Intellectual disability
(133)
Human disease
(14)
Hereditary neurological disease
(6)
Disease of genetic or genomic mechanism
(2)
Autosomal dominant disease
(0)
Autosomal dominant non-syndromic intellectual disability
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.