Disease #00453 (Perry (Perry syndrome), OMIM:168605)
| Official abbreviation |
Perry |
| Name |
Perry syndrome |
| OMIM ID |
168605 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
8 |
| Associated with 1 gene |
DCTN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-11 12:07:56 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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