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Coffin-Siris syndrome

Coffin-Siris syndrome (CSS) is a rare congenital multi-systemic genetic disorder characterized by aplasia or hypoplasia of the distal phalanx or nail of the fifth digit, developmental delay, intellectual disability, coarse facial features, and other variable clinical manifestations.

1 trial tagged with this condition →

Coffin-Siris syndrome 1 0 trials
Coffin-Siris syndrome 10 0 trials
Coffin-Siris syndrome 11 0 trials
Coffin-Siris syndrome 12 0 trials
Coffin-Siris syndrome 5 0 trials
Coffin-Siris syndrome 7 0 trials
Coffin-Siris syndrome 8 0 trials
Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism 0 trials
Intellectual disability, autosomal dominant 14 0 trials
Intellectual disability, autosomal dominant 15 0 trials
Intellectual disability, autosomal dominant 16 0 trials