Hyperthyroxinemia, familial dysalbuminemic
Information
- Disease name
- Hyperthyroxinemia, familial dysalbuminemic
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- MedGen concept unique identifier (MedGen Concept name)
- C0342185
- MedGen unique identifier (MedGen Concept name)
- 90974
- MeSH unique ID (MeSH (Medical Subject Headings))
- D050010