# Albright's hereditary osteodystrophy

> osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face

**Wikidata**: [Q4712685](https://www.wikidata.org/wiki/Q4712685)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Albright's_hereditary_osteodystrophy)  
**Source**: https://4ort.xyz/entity/albright-s-hereditary-osteodystrophy


## References

1. Disease Ontology
2. Sinus pauses and high-grade atrioventricular block in Albright's hereditary osteodystrophy with pseudopseudohypoparathyroidism
3. Monarch Disease Ontology release 2018-06-29
4. [Source](http://www.bartleby.com/107/illus708.html)
5. UniProt
6. Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000087460/MONDO_0007078)
8. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000087460/Orphanet_665)
9. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)
10. [Source](https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx)