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Hemophilia B Leyden

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ORPHA:617930

Classification level: Subtype of disorder

Synonym(s):
  • Factor IX deficiency, Leyden type
  • F9 deficiency, Leyden type

Source: PubMed ID 34168126 5450691 1631558

Prevalence: -

Inheritance: -

Age of onset:

ICD-10: D67

ICD-11: 3B11.Y

UMLS: C5848256

MedDRA: 10016077

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

Guidelines
Emergency guidelines
Français (2022.pdf) - Orphanet Urgences
Deutsch (2009.pdf) - Orphanet Urgences
Italiano (2009.pdf) - Orphanet Urgences
Clinical practice guidelines
Disease review articles
Review article
English (2025) - Lancet
The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.