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Disease Ontology Browser
CODAS syndrome (DOID:0111274)
Alliance: disease page
Synonyms: cerebral, ocular, dental, auricular, and skeletal syndrome; cerebro-oculo-dento-auriculo-skeletal syndrome
Alt IDs: OMIM:600373, MESH:C536434, ORDO:1458, UMLS_CUI:C1838180
Definition: A syndrome characterized by developmental delay, and cerebral, ocular, dental, auricular, and skeletal anomalies that has_material_basis_in homozygous or compound heterozygous mutation in LONP1 on 19p13.3.


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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last database update
02/11/2020
MGI 6.14
The Jackson Laboratory