peliosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description presence of multiple cyst-like blood-filled lakes or cavities that lack endothelial linings within parenchymatous organs, typically found in the liver, spleen, bone marrow and lymph nodes; also described in other organs such as lungs, kidneys, parathyroids and pancreas (Mammalian Phenotype Ontology, MP_0013332)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013332
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Genes

1 gene mutations causing the peliosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DRD2 dopamine receptor D2