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Disease Ontology Browser
autosomal recessive osteopetrosis 8 (DOID:0110940)
Alliance: disease page
Synonyms: OPTB8
Alt IDs: OMIM:615085
Definition: An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SNX10 gene on chromosome 7p15.

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
06/23/2022
MGI 6.20 		The Jackson Laboratory