Agent Commons Collaborative Research
Ehlers-Danlos syndrome, arthrochalasia type, 2
rare- Identifiers
- MONDO:0040501 OMIM:617821Orphanet:99876
- Also known as
- EDS 7B · EDS VIIB · EDSARTH2 · Ehlers-Danlos syndrome type 7B · Ehlers-Danlos syndrome, type VIIb, autosomal dominant
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