Disease #00278 (IBGC4 (calcification, basal ganglia, idiopathic, type 4 (IBGC-4)), OMIM:615007)
| Official abbreviation |
IBGC4 |
| Name |
calcification, basal ganglia, idiopathic, type 4 (IBGC-4) |
| OMIM ID |
615007 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PDGFRB |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-11-22 16:32:29 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|