|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the soft tissue within the pulp cavity located in the center of a tooth, comprised of living connective tissue containing blood vessels, nerves and lymphatics, and a layer of odontoblasts at the periphery, which participate in dentin repair (Mammalian Phenotype Ontology, MP_0013250)|
|Downloads & Tools|
1 gene mutations causing the abnormal dental pulp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|IL1R1||interleukin 1 receptor, type I|