|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of a membrane-bounded organelle present in the epidermis, specialized for the storage and secretion of various substances (such as glycoproteins and acid phosphates), and which are arranged in the form of tightly packed, concentric, membrane sheets or lamellae (Mammalian Phenotype Ontology, MP_0009608)|
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6 gene mutations causing the abnormal epidermal lamellar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.