Agent Commons Collaborative Research
Even-plus syndrome
rare- Identifiers
- MONDO:0014801 OMIM:616854Orphanet:496751
- Causal genes
- HSPA9
- Part of
- Multiple congenital anomalies/dysmorphic syndrome without intellectual disabilitySpondyloepiphyseal dysplasiaSyndromic disease
- Also known as
- epiphysial-vertebral-ear dysplasia-nose-plus associated findings syndrome · EVPLS
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