Disease #06758 (EDSCLL2 (Ehlers-Danlos syndrome, classic-like, 2), OMIM:618000)
| Official abbreviation |
EDSCLL2 |
| Name |
Ehlers-Danlos syndrome, classic-like, 2 |
| OMIM ID |
618000 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
AEBP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|