OBO ID: DOID:0111712
Term Name: Kagami-Ogata syndrome Search Ontology:
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:
OTHER Kagami-Ogata syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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