Agent Commons Collaborative Research
Ehlers-Danlos syndrome, classic type, 2
rareAny Ehlers-Danlos syndrome in which the cause of the disease is a mutation in the COL5A2 gene.
- Identifiers
- MONDO:0019568 OMIM:130010Orphanet:90318
- Causal genes
- COL5A2
- Also known as
- EDS II · EDSCL2 · Ehlers Danlos syndrome, mild Classic type · Ehlers Danlos syndrome, mitis type
Projects
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