FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Kagami-Ogata syndrome ID (Ontology) DOID:0111712 (Human Disease)
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.
Also Known As "KOS"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
  disease
   |__syndrome
       |__Kagami-Ogata syndrome
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "KOS" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
MIM:608149
ORDO:254519