Traits

Traits linked to ADAMTS13

ADAM metallopeptidase with thrombospondin type 1 motif 13

The Human Phenotype Ontology links 20 traits to ADAMTS13, by body system: features seen in people with one of the gene's rare conditions.

Laboratory abnormality

Trait	How often it is seen
Elevated creatinine	Not recorded
Fever	Not recorded
High urine protein levels	Not recorded
Higher than normal levels of lactate in blood	Not recorded
Increased blood urea nitrogen	Not recorded
Small amount of blood in urine	Not recorded

Abnormality of blood and blood-forming tissues

Trait	How often it is seen
Increased immature red blood cells	Not recorded
Low platelet count	Not recorded
Microangiopathic hemolytic anemia	Not recorded
Schistocytosis	Not recorded

Abnormality of the cardiovascular system

Trait	How often it is seen
Mini stroke	Sometimes (5–29%)
Stroke	Sometimes (5–29%)
Heart attack	Rarely (1–4%)

Abnormality of the digestive system

Trait	How often it is seen
Jaundice	Often (30–79%)
Prolonged yellowing of skin in newborn	Not recorded

Abnormality of the genitourinary system

Trait	How often it is seen
Abnormal kidney function	Not recorded
Hemolytic-uremic syndrome	Not recorded

Abnormality of the nervous system

Trait	How often it is seen
Confusion	Not recorded
Tremor	Not recorded

Abnormality of the respiratory system

Trait	How often it is seen
Breathing difficulties	Sometimes (5–29%)

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Where this comes from

The Human Phenotype Ontology, release 2026-09-01: the traits linked to ADAMTS13 and how often each is seen. Find out more at hpo.jax.org.

One test. A lifetime of answers.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test