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DOID:0060241 - 3-M syndrome
Disease Ontology Definition:A syndrome characterized by dwarfism, facial dysmorphia and skeletal abnormalities.
Synonyms: dolichospondylic dysplasia, gloomy face syndrome, Le Merrer syndrome, Miller-McKusick-Malvaux syndrome, three M syndrome, Yakut short stature syndrome
Xenbase Genes
:
obsl1
| MONDO:0007477 - 3-M syndrome |
| MIM:273750 - THREE M SYNDROME 1; 3M1 |
| MIM:612921 - THREE M SYNDROME 2; 3M2 |
| MIM:614205 - THREE M SYNDROME 3; 3M3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
syndrome (is_a)