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Disease Ontology Browser
FICUS syndrome (DOID:0070793)
Alliance: disease page
Synonyms: facial dysmorphism, impaired intellectual development, and cardiac, urogenital, and skeletal anomalies; FICUS
Alt IDs: OMIM:621193, UMLS_CUI:C6011251
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
07/14/2026
MGI 6.24 		The Jackson Laboratory