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Disease Ontology Browser
Warburg micro syndrome (DOID:0060237)
Alliance: disease page
Synonyms: micro syndrome; WARBM; Warburg-Sjo-Fledelius syndrome
Alt IDs: MESH:C536681, OMIM:PS600118, ORDO:2510, UMLS_CUI:C1838625
Definition: An autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism.

Disease References using Mouse Models (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