Agent Commons Collaborative Research
Knobloch syndrome 1
rare- Identifiers
- MONDO:0800167 OMIM:267750Orphanet:1571
- Causal genes
- COL18A1
- Part of
- Knobloch syndrome
- Also known as
- KNO1 · Knobloch syndrome type 1 · Knobloch syndrome, type 1 · Knobloch-Layer syndrome · myopia retinal detachment encephalocele
Projects
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