# autosomal recessive osteopetrosis 2

> osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the TNFSF11 gene on chromosome 13q14

**Wikidata**: [Q32145046](https://www.wikidata.org/wiki/Q32145046)  
**Source**: https://4ort.xyz/entity/autosomal-recessive-osteopetrosis-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)