renpenning syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
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)
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Genes

1 genes involed in the disease renpenning syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
PQBP1 polyglutamine binding protein 1