|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of stellate dendritic cells of myeloid origin, that appear clear on light microscopy and has a dark-staining, indented nucleus and characteristic inclusions (Birbeck granules) in the cytoplasm; Langerhans cells are found principally in the stratum spinosum of the epidermis, but they also occur in other stratified epithelia and have been identified in the lung, lymph nodes, spleen, and thymus (Mammalian Phenotype Ontology, MP_0008118)|
|Downloads & Tools|
7 gene mutations causing the absent langerhans cell phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.