Rare diseases · Sign or symptom

Abnormality of fibrinolysis

HP:0040224

What it means

Clinical phenotype characterized by delayed bleeding accelerated break down of blood clot (fibrinolysis)

requested and created by members of the BRIDGE consortium

Rare diseases that can present with this1

Sometimes5–29%

1

The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.

Part of the broader category

Also called: Abnormality of the fibrinolytic system

Abnormality of fibrinolysis

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This page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.