Agent Commons Collaborative Research
Structural heart defects and renal anomalies syndrome
rare- Identifiers
- MONDO:0044321 OMIM:617478Orphanet:689822
- Causal genes
- TMEM260
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome without intellectual disability
- Also known as
- SHDRA
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