/Coffin-Siris syndrome 6

Coffin-Siris syndrome 6

Rare Disease

MONDO:0033492

Also Known As

ARID2-related BAFopathyCoffin-Siris syndrome 6COFFIN-SIRIS syndrome 6CSS6

Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID2 gene.

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

Coffin-Siris syndrome 1

MONDO:0007617

Baraitser-Winter syndrome 1

MONDO:0009470

intellectual disability-sparse hair-brachydactyly syndrome

MONDO:0011053

intellectual disability, autosomal dominant 22

MONDO:0012869

neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language

MONDO:0013266

intellectual disability, autosomal dominant 14

MONDO:0013819