intracellular accumulation of autofluorescent lipopigment storage material Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The intracellular accumulation of autofluorescent storage material. (Human Phenotype Ontology, HP_0003204)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003204
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Genes

8 genes associated with the intracellular accumulation of autofluorescent lipopigment storage material phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLN3 ceroid-lipofuscinosis, neuronal 3
CLN5 ceroid-lipofuscinosis, neuronal 5
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
KCTD7 potassium channel tetramerization domain containing 7
NDRG1 N-myc downstream regulated 1
TPP1 tripeptidyl peptidase I