/Coffin-Siris syndrome 7

Coffin-Siris syndrome 7

Rare Disease

MONDO:0054831

Also Known As

COFFIN-SIRIS syndrome 7CSS7

Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the DPF2 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

intellectual disability, autosomal dominant 14

MONDO:0013819

intellectual disability, autosomal dominant 15

MONDO:0013820

intellectual disability, autosomal dominant 16

MONDO:0013821

intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism

MONDO:0014376

Coffin-Siris syndrome 5

MONDO:0014838