Coffin-Siris syndrome 7
MONDO:0054831Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the DPF2 gene.
Also known as: COFFIN-SIRIS syndrome 7, CSS7
38 clinical trials for this condition and its sub-types.
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Disease
(618)
Musculoskeletal system disorder
(196)
Hereditary disease
(172)
Syndromic disease
(24)
Human disease
(14)
Developmental defect during embryogenesis
(7)
Skeletal system disorder
(4)
Disease of genetic or genomic mechanism
(2)
Coffin-Siris syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome
(1)