About   Help   FAQ
Disease Ontology Browser
autosomal recessive osteopetrosis 2 (DOID:0110943)
Alliance: disease page
Synonyms: mild autosomal recessive form osteopetrosis; OPTB2; osteoclast-poor osteopetrosis
Alt IDs: OMIM:259710
Definition: An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the TNFSF11 gene on chromosome 13q14.

Disease References using Mouse Models (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
MGI 6.22
The Jackson Laboratory