Disease #03661 (BSVD2;POREN2 (brain small vessel disease, type 2 (BSVD2);porencephaly type 2 (POREN2)), OMIM:614483)
| Official abbreviation |
BSVD2;POREN2 |
| Name |
brain small vessel disease, type 2 (BSVD2);porencephaly type 2 (POREN2) |
| OMIM ID |
614483 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
COL4A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-04-21 11:49:40 +02:00 (CEST) |
Individuals
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