papillary muscle hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in the papillary muscle (Mammalian Phenotype Ontology, MP_0004061)
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1 gene mutations causing the papillary muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MOSPD3 motile sperm domain containing 3