|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||overdevelopment or increased size, usually due to a increased number of cells, outermost layer of the hair follicle that merges proximally with the basal layer of the interfollicular epidermis and distally with the hair bulb (Mammalian Phenotype Ontology, MP_0010688)|
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4 gene mutations causing the hair follicle outer rooth sheath hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.