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Disease Ontology Browser
Malan syndrome (DOID:0112102)
Alliance: disease page
Synonyms: MALNS; SOTOS2; Sotos syndrome 2
Alt IDs: OMIM:614753
Definition: A bone development disease that is characterized by overgrowth, advanced bone age, macrocephaly, and dysmorphic facial features and that has_material_basis_in heterozygous mutation in the NFIX gene on chromosome 19p13.13.

Disease References using Mouse Models (1)
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
09/08/2026
MGI 6.24 		The Jackson Laboratory