Kagami-Ogata syndrome (DOID:0111712)
Alliance: disease page
Synonyms: KOS
Alt IDs: OMIM:608149, ORDO:254519
Definition: A syndrome characterized by polyhydramnios, fetal macrosomia, abdominal wall defects, skeletal abnormalities, feeding difficulties and impaired swallowing, dysmorphic features, developmental delay and intellectual disability that has_material_basis_in heterozygous mutation in an imprinting region on chromosome 14q32.