autosomal recessive osteopetrosis 5

Summary
Synonym
  • OPTB5
  • infantile malignant osteopetrosis 3
Definition
An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in mutation in the OSTM1 gene on chromosome 6q21.
Super Class
autosomal recessive disease osteopetrosis
Disease Ontology
DOID:0110939
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
28962 OSTM1 osteoclastogenesis associated transmembrane protein 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
14628 Ostm1 osteopetrosis associated transmembrane protein 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024