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Disease Ontology Browser
3-M syndrome (DOID:0060241)
Alliance: disease page
Synonyms: dolichospondylic dysplasia; gloomy face syndrome; Le Merrer syndrome; Miller-McKusick-Malvaux syndrome; three M syndrome; Yakut short stature syndrome
Alt IDs: OMIM:273750, OMIM:612921, OMIM:614205, MESH:C535314, MESH:C535725, ORDO:2616, UMLS_CUI:C1848862, UMLS_CUI:C1851996
Definition: An autosomal recessive disease characterized by dwarfism, facial dysmorphia and skeletal abnormalities.


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
06/11/2019
MGI 6.14
The Jackson Laboratory