|OBO ID: DOID:0060248|
|Term Name:||Simpson-Golabi-Behmel syndrome type 1||Search Ontology:|
|Definition:||A syndrome characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities and has_material_basis_in mutation in the gene encoding glypican-3 on chromosome Xq26. (2)|
|Ontology:||Human Disease (DOID:0060248)|
|is a type of:||
OTHER Simpson-Golabi-Behmel syndrome type 1 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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