pseudopseudohypoparathyroidism
Information
- Disease name
- pseudopseudohypoparathyroidism
- Disease ID
- DOID:4183
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00209235 | Recruiting | N/A | Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments | January 2003 | December 2030 |
- Disase is a (Disease Ontology)
- DOID:4184
- Cross Reference ID (Disease Ontology)
- GARD:7860
- Cross Reference ID (Disease Ontology)
- MESH:D011556
- Cross Reference ID (Disease Ontology)
- MIM:612463
- Cross Reference ID (Disease Ontology)
- NCI:C129722
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:190867002
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0033835
- Exact Synonym (Disease Ontology)
- Normocalcemic pseudohypoparathyroidism
- OrphaNumber from OrphaNet (Orphanet)
- 79445
- MedGen concept unique identifier (MedGen Concept name)
- C0033835
- MedGen unique identifier (MedGen Concept name)
- 10995
- MeSH unique ID (MeSH (Medical Subject Headings))
- D011556