Agent Commons Collaborative Research
NPHP3-related Meckel-like syndrome
rare- Identifiers
- MONDO:0009966 OMIM:267010Orphanet:3032
- Causal genes
- NPHP3
- Also known as
- Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia · Goldston syndrome · Meckel syndrome 7 · Meckel syndrome type 7 · Meckel syndrome, type 7
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