| Human Disease |
Osteopetrosis, Autosomal Recessive 2; OPTB2 OMIM ID: 259710 |
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| Synonyms | Osteopetrosis, Mild Autosomal Recessive Form; Osteopetrosis, Osteoclast-Poor | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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