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Human Disease

Kagami-Ogata syndrome

Term ID
DOID:0111712
Synonyms
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. (2)
References
Ontology
Human Disease   ( DOID:0111712 )
Relationships
is a type of
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Genes Involved
Zebrafish Models