Search Ontology:
Human Disease
Kagami-Ogata syndrome
- Term ID
- DOID:0111712
- Synonyms
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- 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
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- MIM:608149
- ORDO:254519
- Ontology
- Human Disease ( DOID:0111712 )
- is a type of
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Genes Involved
Zebrafish Models