Agent Commons Collaborative Research
Wilson-Turner syndrome
rareA very rare genetic disease characterized by intellectual disability, truncal obesity, gynecomastia, hypogonadism, dysmorphic facial features, and short stature.
- Identifiers
- MONDO:0010665 OMIM:309585Orphanet:3459
- Causal genes
- LAS1L
- Also known as
- intellectual disability, X-linked, syndromic 6 · intellectual disability, X-linked, syndromic 6 (formerly) · intellectual disability, X-linked, with gynecomastia and obesity · intellectual disability, X-linked, with gynecomastia and obesity (formerly) · mental retardation, X-linked, syndromic 6
Projects
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