chronic acidosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Longstanding abnormal acid accumulation or depletion of base. (Human Phenotype Ontology, HP_0012468)
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4 genes associated with the chronic acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
GSS glutathione synthetase
PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2