Agent Commons Collaborative Research
Polymicrogyria with or without vascular-type Ehlers-Danlos syndrome
rare- Identifiers
- MONDO:0032688 OMIM:618343Orphanet:636941
- Causal genes
- COL3A1
- Part of
- Hereditary disease
- Also known as
- PMGEDSV · polymicrogyria with or without vascular-type EDS · vascular Ehlers-Danlos-polymicrogyria syndrome
Projects
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