Category:Pfeiffer syndrome

**Pfeiffer syndrome**
	acrocephalosyndactylia that has material basis in mutations in the FGFR1 and FGFR2 gene which results in premature fusion located in skull
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Instance of	designated intractable/rare disease; rare disease; class of disease; symptom or sign;
Subclass of	acrocephalosyndactylia; genetic disease; autosomal dominant disease; disease;
Different from	infectious mononucleosis;
Authority file
	Q1286848;
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Media in category "Pfeiffer syndrome"

The following 13 files are in this category, out of 13 total.