Metadata | |
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ID | DOID:0111712 |
Name | Kagami-Ogata syndrome |
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. https://www.ncbi.nlm.nih.gov/pubmed/10951461, https://www.ncbi.nlm.nih.gov/pubmed/12938037 |
Xrefs | |
Subsets |
DO_rare_slim |
Synonyms |
KOS [EXACT] |
Parent Relationships |
is_a syndrome |