Disease #01699 (IBGC1 (calcification, basal ganglia, idiopathic, type 1 (IBGC-1, Fahr's syndrome)), OMIM:213600)
| Official abbreviation |
IBGC1 |
| Name |
calcification, basal ganglia, idiopathic, type 1 (IBGC-1, Fahr's syndrome) |
| OMIM ID |
213600 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
25 |
| Phenotype entries for this disease |
25 |
| Associated with 1 gene |
SLC20A2 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|