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- Bdc3741355841ee65979c9a1949302182 hasDbXref "GARD:0003160" @default.
- Bdc3741355841ee65979c9a1949302182 type Axiom @default.
- Bdc3741355841ee65979c9a1949302182 annotatedProperty IAO_0000115 @default.
- Bdc3741355841ee65979c9a1949302182 annotatedSource MONDO_0013047 @default.
- Bdc3741355841ee65979c9a1949302182 annotatedTarget "A condition that affects how the body breaks down sugar to use as energy in muscle cells. People withthis conditionexperience fatigue, muscle pain, and cramps during exercise (exercise intolerance). In some people,high-intensity exercise or other strenuous activity leads to the breakdown of muscle tissue (rhabdomyolysis), which can lead to myoglobinuria (rust-colored urine indicating breakdown of muscle tissue) and kidney damage. A skin rash may also develop. The severity of the signs and symptoms varies greatly among affected individuals. Lactate dehydrogenase A deficiency is caused by mutations in the LDHA gene. This condition is inherited in an autosomal recessive pattern." @default.