increased extraneuronal autofluorescent lipopigment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lipofuscin, a generic term applied to autofluorescent lipopigment, is a mixture of protein and lipid that accumulates in most aging cells, particularly those involved in high lipid turnover (e.g., the adrenal medulla) or phagocytosis of other cell types (e g., the retinal pigment epithelium or RPE; macrophage). This term pertains if there is an increase in the extraneuronal accumulation of lipofuscin (also known as autofluorescent lipoprotein) more than expected for the age of the patient. (Human Phenotype Ontology, HP_0003463)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003463
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Genes

2 genes associated with the increased extraneuronal autofluorescent lipopigment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLN3 ceroid-lipofuscinosis, neuronal 3
TPP1 tripeptidyl peptidase I