Disease #03677 (IBGC (calcification, basal ganglia, idiopathic (IBGC)), OMIM:614540)
| Official abbreviation |
IBGC |
| Name |
calcification, basal ganglia, idiopathic (IBGC) |
| OMIM ID |
614540 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
11 |
| Phenotype entries for this disease |
11 |
| Associated with 1 gene |
SLC20A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-02-11 08:59:45 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|