autosomal recessive osteopetrosis 2

Summary
Synonym
  • OPTB2
  • mild autosomal recessive form osteopetrosis
  • osteoclast-poor osteopetrosis
Definition
An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the TNFSF11 gene on chromosome 13q14.
Super Class
autosomal recessive disease osteopetrosis
Disease Ontology
DOID:0110943
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8600 TNFSF11 TNF superfamily member 11
Displaying 1 entry
Gene ID Gene Symbol Description Source
21943 Tnfsf11 tumor necrosis factor (ligand) superfamily, member 11
Displaying 1 entry
Gene ID Gene Symbol Description Source
117516 Tnfsf11 TNF superfamily member 11

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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