Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism
MONDO:0014376Also known as: CSS9, Coffin-Siris syndrome 9, MRD27, autosomal dominant intellectual disability 27, intellectual disability, autosomal dominant 27, intellectual disability, autosomal dominant type 27, mental retardation, autosomal dominant type 27, autosomal dominant non-syndromic intellectual disability 27
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)