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- Bc6026a373b1a1b44c6e8c7ba767ff967 hasDbXref "https://www.clinicalgenome.org/affiliation/40026" @default.
- Bc6026a373b1a1b44c6e8c7ba767ff967 type Axiom @default.
- Bc6026a373b1a1b44c6e8c7ba767ff967 annotatedProperty IAO_0000115 @default.
- Bc6026a373b1a1b44c6e8c7ba767ff967 annotatedSource MONDO_0010480 @default.
- Bc6026a373b1a1b44c6e8c7ba767ff967 annotatedTarget "An X-linked genetic condition caused by alterations in the gene G6PD that result in severely decreased activity levels of the enzyme glucose-6-phosphate dehydrogenase. Individuals with hemizygous G6PD variants associated with CNSHA have CNSHA. Individuals with G6PD variants that cause CNSHA are at risk for acute hemolytic anemia in response to certain medication exposures, chemical exposures, infections, or consumption of fava beans." @default.