Disease #05817 (EDSCL2 (Ehlers-Danlos, classic syndrome, type 2 (EDSCL2 EDS2)), OMIM:130010)
| Official abbreviation |
EDSCL2 |
| Name |
Ehlers-Danlos, classic syndrome, type 2 (EDSCL2 EDS2) |
| OMIM ID |
130010 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
13 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
COL5A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-08-24 11:20:25 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|