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Disease Ontology Browser
autosomal recessive osteopetrosis 5 (DOID:0110939)
Alliance: disease page
Synonyms: infantile malignant osteopetrosis 3; OPTB5
Alt IDs: OMIM:259720
Definition: An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in mutation in the OSTM1 gene on chromosome 6q21.

Disease References using Mouse Models (1)
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory