Traits

Traits linked to SLC25A13

solute carrier family 25 member 13

The Human Phenotype Ontology links 94 traits to SLC25A13, by body system: features seen in people with one of the gene's rare conditions.

Laboratory abnormality

Trait	Kaip dažnai pasireiškia
Conjugated hyperbilirubinemia	Visada
Elevated alkaline phosphatase	Visada
Elevated blood lysine	Visada
Elevated circulating alanine aminotransferase concentration	Visada
Elevated circulating aspartate aminotransferase concentration	Visada
Elevated circulating citrulline concentration	Visada
Elevated gamma-glutamyltransferase level	Visada
High blood arginine levels	Visada
High blood bilirubin levels	Visada
High blood threonine levels	Visada
Increased methionine in blood	Visada
Increased serum bile acid concentration	Visada
Increased tyrosine in blood	Visada
Macrovesicular hepatic steatosis	Visada
Microvesicular hepatic steatosis	Visada
Abnormal circulating lipid concentration	Labai dažnai (80–99%)
Acute hyperammonemia	Labai dažnai (80–99%)
Elevated circulating alpha-fetoprotein concentration	Labai dažnai (80–99%)
Fatty infiltration of liver	Labai dažnai (80–99%)
Hypergalactosemia	Labai dažnai (80–99%)
Increased circulating lactate dehydrogenase concentration	Labai dažnai (80–99%)
Increased lactate in body	Labai dažnai (80–99%)
Increased plasma triglycerides	Labai dažnai (80–99%)
Low albumin	Labai dažnai (80–99%)
Abnormal circulating alanine concentration	Dažnai (30–79%)
Abnormal circulating arginine concentration	Dažnai (30–79%)
Abnormal circulating glutamine concentration	Dažnai (30–79%)
Decreased protein levels in blood	Dažnai (30–79%)
Elevated lipids in blood	Dažnai (30–79%)
High blood ammonia levels	Dažnai (30–79%)
High liver enzymes	Dažnai (30–79%)
Abnormal circulating serine concentration	Kartais (5–29%)
Brain swelling	Kartais (5–29%)
Decreased circulating high-density lipoprotein cholesterol	Kartais (5–29%)
Elevated serum cholesterol	Kartais (5–29%)
Increased circulating LDL level	Kartais (5–29%)
Increased urinary glycerol	Kartais (5–29%)
Ketonuria	Kartais (5–29%)
Argininosuccinic aciduria	Neužfiksuota

Abnormality of the nervous system

Trait	Kaip dažnai pasireiškia
Abnormal eating behavior	Dažnai (30–79%)
Aggressive behavior	Dažnai (30–79%)
Asterixis	Dažnai (30–79%)
Confusion	Dažnai (30–79%)
Delirium	Dažnai (30–79%)
Delusions	Dažnai (30–79%)
Difficulty sleeping	Dažnai (30–79%)
Drowsiness	Dažnai (30–79%)
Epilepsy	Dažnai (30–79%)
Fluctuations in consciousness	Dažnai (30–79%)
Hallucinations	Dažnai (30–79%)
Irritability	Dažnai (30–79%)
Lethargy	Dažnai (30–79%)
Memory impairment	Dažnai (30–79%)
Restlessness	Dažnai (30–79%)
Tremor	Dažnai (30–79%)
Waking up screaming	Dažnai (30–79%)
Coma	Kartais (5–29%)
Difficulty staying or falling asleep	Kartais (5–29%)
Echoing another person's speech	Kartais (5–29%)
Global developmental delay	Kartais (5–29%)
Hepatic encephalopathy	Kartais (5–29%)
Manic	Kartais (5–29%)
More active than typical	Kartais (5–29%)
Psychosis	Kartais (5–29%)
Protein craving	Neužfiksuota

Abnormality of the digestive system

Trait	Kaip dažnai pasireiškia
Portal fibrosis	Visada
Jaundice	Labai dažnai (80–99%)
Slowed or blocked flow of bile from liver	Labai dažnai (80–99%)
Diarrhea	Dažnai (30–79%)
Enlarged liver	Dažnai (30–79%)
Hepatic fibrosis	Dažnai (30–79%)
Portal inflammation	Dažnai (30–79%)
Ballooning hepatocyte degeneration	Kartais (5–29%)
Hepatocellular carcinoma	Kartais (5–29%)
Pancreatic inflammation	Kartais (5–29%)
Poor appetite	Kartais (5–29%)
Vomiting	Kartais (5–29%)
Impaired release of bile from liver	Neužfiksuota
Scar tissue replaces healthy tissue in the liver	Neužfiksuota

Growth abnormality

Trait	Kaip dažnai pasireiškia
Decreased body mass index	Labai dažnai (80–99%)
Faltering weight in infancy	Dažnai (30–79%)
Prenatal growth deficiency	Kartais (5–29%)
Faltering weight	Neužfiksuota
Growth delay	Neužfiksuota

Abnormality of blood and blood-forming tissues

Trait	Kaip dažnai pasireiškia
Prolonged prothrombin time	Labai dažnai (80–99%)
Gastrointestinal bleeding	Kartais (5–29%)
Low number of red blood cells or hemoglobin	Kartais (5–29%)
Bleeding tendency	Retai (1–4 %)

Abnormal cellular phenotype

Trait	Kaip dažnai pasireiškia
Decreased circulating antibody level	Labai dažnai (80–99%)

Abnormality of the cardiovascular system

Trait	Kaip dažnai pasireiškia
Enlarged liver and spleen	Dažnai (30–79%)

Abnormality of the endocrine system

Trait	Kaip dažnai pasireiškia
Delayed start of first period	Kartais (5–29%)

Abnormality of the eye

Trait	Kaip dažnai pasireiškia
Clouding of the lens of the eye	Retai (1–4 %)

Abnormality of the genitourinary system

Trait	Kaip dažnai pasireiškia
Enuresis	Kartais (5–29%)

Constitutional symptom

Trait	Kaip dažnai pasireiškia
Night sweats	Dažnai (30–79%)

Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.

Iš kur tai žinoma

The Human Phenotype Ontology, release 2026-09-01: the traits linked to SLC25A13 and how often each is seen. Find out more at hpo.jax.org.

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