Term Name: | Roberts syndrome |
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Synonyms: | LONG BONE DEFICIENCIES ASSOCIATED WITH CLEFT LIP-PALATE, RBS, Roberts-Sc Phocomelia Syndrome, SC phocomelia syndrome |
Definition: | A syndrome characterized by tetraphocomelia, craniofacial anomalies, growth retardation, intellectual disability, and cardiac and renal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the ESCO2 gene on chromosome 8p21.1. |
Ontology: | Human Disease [DOID:5325] ( DOID:5325 ) |