Early-onset immune dysregulation

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Early-onset immune dysregulation due to DOCK11 complete deficiency

ORPHA:658951Disease

Also called Early-onset immune dysregulation due to dedicator of cytokinesis 11 protein complete deficiency

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Prevalence
<1 / 1 000 000
Age of onset
Childhood, Infancy
Inheritance
X-linked recessive
Classified as
Disease

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Gene

DOCK11Disease-causing germline mutation(s) (loss of function)

ICD-10 codes

D89.8filed under a broader ICD-10 category — shared with 29 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MONDO 0958138MONDO 958138OMIM 301109UMLS C5925136

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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