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Disease Ontology Browser
autosomal recessive osteopetrosis 5 (DOID:0110939)
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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/20/2017
MGI 6.10
The Jackson Laboratory