abnormality of epidermal morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the morphology of the epidermis. (Human Phenotype Ontology, HP_0011124)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011124
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Genes

5 genes associated with the abnormality of epidermal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1
DSG1 desmoglein 1
DSP desmoplakin
HLA-B major histocompatibility complex, class I, B
KRT2 keratin 2, type II