10 relations: Acute kidney injury, Adenine phosphoribosyltransferase, Autosome, Dominance (genetics), Genetic carrier, Kidney, Kidney stone disease, Metabolic disorder, Purine, 2,8-Dihydroxyadenine.
Acute kidney injury
Acute kidney injury (AKI), previously called acute renal failure (ARF), is an abrupt loss of kidney function that develops within 7 days.
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Adenine phosphoribosyltransferase
Adenine phosphoribosyltransferase (APRTase) is an enzyme encoded by the APRT gene, found in humans on chromosome 16.
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Autosome
An autosome is a chromosome that is not an allosome (a sex chromosome).
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Dominance (genetics)
Dominance in genetics is a relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus.
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Genetic carrier
A hereditary carrier (or just carrier), is a person or other organism that has inherited a recessive allele for a genetic trait or mutation but usually does not display that trait or show symptoms of the disease.
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Kidney
The kidneys are two bean-shaped organs present in left and right sides of the body in vertebrates.
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Kidney stone disease
Kidney stone disease, also known as urolithiasis, is when a solid piece of material (kidney stone) occurs in the urinary tract.
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Metabolic disorder
A metabolic disorder can happen when abnormal chemical reactions in the body alter the normal metabolic process.
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Purine
A purine is a heterocyclic aromatic organic compound that consists of a pyrimidine ring fused to an imidazole ring.
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2,8-Dihydroxyadenine
2,8-Dihydroxyadenine is a derivative of adenine which accumulates in 2,8 dihydroxy-adenine urolithiasis.
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Redirects here:
2,8 dihydroxy-adenine urolithiasis, 2,8 dihydroxyadenine urolithiasis, 2,8-dihydroxyadeninuria, APRT deficiency.
References
[1] https://en.wikipedia.org/wiki/Adenine_phosphoribosyltransferase_deficiency