Disease #00059 (EDSCL2 (EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2), OMIM:130010)
| Official abbreviation |
EDSCL2 |
| Name |
EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2 |
| OMIM ID |
130010 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
AEBP1, COL5A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2022-06-29 14:10:15 +00:00 (UTC) |
| Date last edited |
2023-06-16 09:07:03 +00:00 (UTC) |
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