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Congenital hypofibrinogenemia

ORPHA: 101041

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Clinical Presentation

Signs and symptoms associated with Congenital hypofibrinogenemia, sourced from HPO and Orphanet clinical annotations.

Gingival bleedingEpistaxisAbnormal bleedingGastrointestinal hemorrhage

Classification & Codes

Orphanet Code

ORPHA:101041
Congenital hypofibrinogenemia
OrphanetORPHA:101041
Treatments0 drug(s)
Symptoms on record4 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO