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Disease Ontology Browser
distal arthrogryposis (DOID:0050646)
Synonyms: Arthrogryposis Multiplex Congenita; Freeman-Sheldon syndrome; Freeman-Sheldon syndrome variant; Sheldon-Hall syndrome
Alt IDs: OMIM:108120, OMIM:108145, OMIM:108200, OMIM:114300, OMIM:121050, OMIM:121070, OMIM:158300, OMIM:178110, OMIM:187370, OMIM:193700, OMIM:601680, OMIM:609128, OMIM:614335, OMIM:615065, ORDO:1147, ORDO:97120
Definition: A muscle tissue disease characterized by congenital joint contractures of hand and feet.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/13/2017
MGI 6.10
The Jackson Laboratory