renpenning syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males. (Human Disease Ontology, DOID_0060179)
External Link http://www.omim.org/entry/309500
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Genes

1 genes associated with the renpenning syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PQBP1 polyglutamine binding protein 1