Disease #02894 (Polymicrogyria, asymmetric, OMIM:610031)
| Official abbreviation |
- |
| Name |
Polymicrogyria, asymmetric |
| OMIM ID |
610031 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TUBB2B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|