Disease #05067 (IBGC6 (calcification, basal ganglia, idiopathic, type 6 (IBGC-6)), OMIM:616413)
| Official abbreviation |
IBGC6 |
| Name |
calcification, basal ganglia, idiopathic, type 6 (IBGC-6) |
| OMIM ID |
616413 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
XPR1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 11:00:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|