Category:Coffin-Siris syndrome

**Coffin-Siris syndrome**
	genetic disease that is characterized by underdevelopment of the tips of fingers or toes, underdevelopment or abscense of finger or toe nails and developmental disability Noi de 16 anys amb la síndrome de Coffin-Siris amb mutacions en el gen ARID1B, mostrant una discreta microcefàlia
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Instance of	rare disease; class of disease;
Subclass of	syndrome; autosomal dominant non-syndromic intellectual disability;
Named after	Grange S. Coffin;
Authority file
	Q2348105;
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Media in category "Coffin-Siris syndrome"

The following 3 files are in this category, out of 3 total.