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Traits

Traits linked to AGXT

alanine--glyoxylate aminotransferase

The Human Phenotype Ontology links 43 traits to AGXT, by body system: features seen in people with one of the gene's rare conditions.

Abnormality of the genitourinary system

TraitCât de frecvent apare
Increased calcium level in kidneyÎntotdeauna
Renal failureÎntotdeauna
Kidney stoneFoarte des (80–99%)
Decreased glomerular filtration rateDes (30–79%)
Dull burning sensation with urinationDes (30–79%)
EnuresisUneori (5–29%)
Frequent urinary tract infectionsUneori (5–29%)
Stage 5 chronic kidney diseaseUneori (5–29%)
Calcium oxalate nephrolithiasisNeînregistrat

Laboratory abnormality

TraitCât de frecvent apare
DehydrationÎntotdeauna
Elevated urinary glycolic acid levelÎntotdeauna
Elevated urinary glyoxylic acid levelÎntotdeauna
High urine oxalate levelsÎntotdeauna
Abnormal circulating enzyme concentrationFoarte des (80–99%)
Metabolic acidosisFoarte des (80–99%)
Blood in urineDes (30–79%)
Laboratory abnormalityRar (1–4%)
Reduced hepatic alanine-glyoxylate aminotransferase activityNeînregistrat

Abnormality of the cardiovascular system

TraitCât de frecvent apare
Narrowing and hardening of arteriesRar (1–4%)
StrokeRar (1–4%)
Arterial occlusionNeînregistrat
Cutis marmorataNeînregistrat
Intermittent claudicationNeînregistrat
Interruption of electrical communication between upper and lower chambers of heartNeînregistrat
Peripheral arterial stenosisNeînregistrat
Raynaud phenomenonNeînregistrat

Abnormality of the musculoskeletal system

TraitCât de frecvent apare
Calcium buildup in soft tissues of bodyFoarte des (80–99%)
Abnormality of the skeletal systemUneori (5–29%)
Bone painNeînregistrat
Calcinosis cutisNeînregistrat
Increased bone mineral densityNeînregistrat
Spontaneous fractureNeînregistrat

Abnormality of the eye

TraitCât de frecvent apare
Choroidal neovascularizationNeînregistrat
Damaged optic nerveNeînregistrat
Noninflammatory retina diseaseNeînregistrat
Optic atrophyNeînregistrat
Retinal crystalsNeînregistrat

Abnormality of blood and blood-forming tissues

TraitCât de frecvent apare
Low number of red blood cells or hemoglobinFoarte des (80–99%)

Abnormality of head or neck

TraitCât de frecvent apare
Abnormal dentitionRar (1–4%)

Abnormality of the integument

TraitCât de frecvent apare
Persistent blue color of hands or feetNeînregistrat

Abnormality of the nervous system

TraitCât de frecvent apare
Peripheral neuropathyNeînregistrat

Constitutional symptom

TraitCât de frecvent apare
Death of body tissue due to lack of blood flow or infectionNeînregistrat

Growth abnormality

TraitCât de frecvent apare
Faltering weightDes (30–79%)

Cât de frecvent apare în rândul persoanelor cu una dintre afecțiunile asociate genei, cel mai des întâlnit dintre acestea, conform Human Phenotype Ontology. Aceste pagini descriu trăsături și cercetările din spatele lor; ele nu reprezintă un diagnostic, iar pentru simptome trebuie să vă adresați medicului sau consilierului genetic.

De unde provin aceste informații

  • The Human Phenotype Ontology, release 2026-09-01: the traits linked to AGXT and how often each is seen. Find out more at hpo.jax.org.

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