Term Name: Roberts syndrome
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 )

Relationships
is a type of: autosomal recessive disease syndrome