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Disease Ontology Browser
Larsen syndrome (DOID:14764)
Alliance: disease page
Synonyms: dominant larsen syndrome
Alt IDs: OMIM:150250
Definition: Asyndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial 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
10/12/2021
MGI 6.17
The Jackson Laboratory