Term Name:	FICUS syndrome
Synonyms:	facial dysmorphism, impaired intellectual development, and cardiac, urogenital, and skeletal anomalies, FICUS
Definition:	An autosomal recessive intellectual developmental disorder characterized by dysmorphic facial features, impaired intellectual development, and multisystem features including cardiovascular, urogenital, skeletal, gastrointestinal, and ophthalmologic abnormalities that has_material_basis_in homozygous mutation in the LSM1 gene on chromosome 8p11.
Ontology:	Human Disease [DOID:0070793]   ( DOID:0070793 )