Category:Greig syndrome

**Greig cephalopolysyndactyly syndrome**
	acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face
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Instance of	developmental defect during embryogenesis; rare disease; class of disease;
Subclass of	acrocephalosyndactylia; syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy; genetic disease; autosomal dominant disease;
Named after	David Middleton Greig;
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	Q3508649;
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