insidious onset Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Gradual, very slow onset of disease manifestations. (Human Phenotype Ontology, HP_0003587)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003587
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Genes

8 genes associated with the insidious onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL1 atlastin GTPase 1
EIF4G1 eukaryotic translation initiation factor 4 gamma, 1
KIAA0196 KIAA0196
MPZ myelin protein zero
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
OPA1 optic atrophy 1 (autosomal dominant)
PMP22 peripheral myelin protein 22
SPAST spastin