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Disease Ontology Browser
Smith-Lemli-Opitz syndrome (DOID:14692)
Alliance: disease page
Synonyms: Rutledge lethal multiple congenital anomaly syndrome; Smith-Opitz-Inborn syndrome
Alt IDs: OMIM:270400, DOID:4366, ICD10CM:E78.72, MESH:D019082, NCI:C85071, UMLS_CUI:C0175694

Disease References using Mouse Models (5)

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
MGI 6.17
The Jackson Laboratory