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Disease Ontology Browser
Galloway-Mowat syndrome (DOID:0060364)
Alliance: disease page
Synonyms: Galloway syndrome; microcephaly, hiatal hernia and nephrotic syndrome; nephrosis-microcephaly syndrome; nephrosis-neuronal dysmigration syndrome
Alt IDs: OMIM:251300, MESH:C537548, NCI:C132195, ORDO:2065, UMLS_CUI:C0795949
Definition: A syndrome characterized_by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome.


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
05/26/2020
MGI 6.15
The Jackson Laboratory