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Standards Ontologies Notations
Keshan disease

Summary
Definition
A nutritional deficiency that is disease characterized by a cardiomyopathy secondary to selenium deficiency.
Super Class
nutritional deficiency disease
Disease Ontology
DOID:0050083
Mondo Disease Ontology
MeSH
GARD
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
1543 CYP1A1 cytochrome P450 family 1 subfamily A member 1
1557 CYP2C19 cytochrome P450 family 2 subfamily C member 19
2876 GPX1 glutathione peroxidase 1
Displaying all 3 entries
Gene ID Gene Symbol Description Source
13076 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1
13095 Cyp2c29 cytochrome P450, family 2, subfamily c, polypeptide 29
14775 Gpx1 glutathione peroxidase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
24296 Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
181178 gpx-5 Glutathione peroxidase
182513 gpx-3 Glutathione peroxidase 3
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Last updated: December 9, 2024