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
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