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Summary Literature (0)
DOID:0060241 - 3-M syndrome

Disease Ontology Definition:An autosomal recessive disease characterized by dwarfism, facial dysmorphia and skeletal abnormalities.

Synonyms: Le Merrer syndrome, Miller-McKusick-Malvaux syndrome, Yakut short stature syndrome, dolichospondylic dysplasia, gloomy face syndrome, three M syndrome

Echinobase Genes :

OMIM:612921 - three m syndrome 2; 3m2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a)