About   Help   FAQ
Disease Ontology Browser
hereditary arterial and articular multiple calcification syndrome (DOID:0111582)
Alliance: disease page
Synonyms: arterial calcification and distal joint calcification; arterial calcification due to CD73 deficiency; arterial calcification due to deficiency of CD73; calcification of joints and arteries; CALJA
Alt IDs: OMIM:211800, ORDO:289601
Definition: A syndrome characterized by adult onset of calcification of arteries in the lower extremities and of the hand and foot capsule joints that has_material_basis_in homozygous or compound heterozygous mutation in the NT5E gene on chromosome 6q14.3.

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory