Kagami-Ogata Syndrome
Disease ID: disease_node_20385
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| Dbxref | MIM:608149, ORDO:254519 |
|---|---|
| Subclassof | DOID_225 |
| Data Source | DOID |
| Synonyms | KOS |
| Doid Label | Kagami-Ogata syndrome |
| Doid Description | 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. |
| Disease Node Id | disease_node_20385 |
| Doid Id | DOID_0111712 |
| Label | Kagami-Ogata Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)