ECRD 2026

Knowledge on rare diseases and orphan drugs

COVID-19 & Rare diseases logo Rare Diseases Resources for Refugees/Displaced Persons
Homepage > Rare diseases > Search

Search for a rare disease

*
(*) mandatory field

NFKB1-related immune dysregulation

Suggest an update
Your message has been sent Your message has not been sent. Please contact an administrator.

ORPHA:696874

Classification level: Disorder

Synonym(s):
  • Nuclear factor kappa B subunit 1-related immune dysregulation

Source: PubMed ID 16639407 36356849 32278790

Prevalence: -

Inheritance: Autosomal dominant

Age of onset:

ICD-10: D81.8

ICD-11: 4A01.2Y

OMIM: 616576

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 (2020.pdf) - Orphanet Urgences
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

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.