Albright's hereditary osteodystrophy
Information
- Disease name
- Albright's hereditary osteodystrophy
- Disease ID
- DOID:0080053
- Description
- "An pseudohypoparathyroidism 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." [url:http\://en.wikipedia.org/wiki/Albright%27s_hereditary_osteodystrophy, url:http\://rarediseases.info.nih.gov/GARD/Disease.aspx?diseaseID=5770, url:http\://www.orpha.net/data/patho/Pro/en/Albright-FRenPro1314.pdf]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:4184
- Cross Reference ID (Disease Ontology)
- GARD:5770
- Cross Reference ID (Disease Ontology)
- MESH:C537045
- Cross Reference ID (Disease Ontology)
- MIM:103580
- Exact Synonym (Disease Ontology)
- Albright hereditary osteodystrophy
- Exact Synonym (Disease Ontology)
- pseudohypoparathyroidism type 1a