Chronic mucocutaneous candidiasis

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Chronic mucocutaneous candidiasis

ORPHA:1334Disease

Also called CMC

What it is

A rare primary immunodeficiency characterized by persistent, debilitating and/or recurrent infections of the skin, nails, and mucus membranes, mainly with the fungal pathogen Candida albicans.

Key facts

Age of onset
Childhood, Infancy
Inheritance
Autosomal dominant, Autosomal recessive
Classified as
Disease

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Genes

CLEC7ADisease-causing germline mutation(s)
IL17FDisease-causing germline mutation(s)
IL17RADisease-causing germline mutation(s)
IL17RCDisease-causing germline mutation(s) (loss of function)
TRAF3IP2Disease-causing germline mutation(s)

ICD-10 codes

B37.2filed under a broader ICD-10 category

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

GARD 1077MEDDRA 10009007MESH D002178MONDO 0015279OMIM 114580OMIM 247650OMIM 252250OMIM 607644OMIM 613108OMIM 613953OMIM 613956OMIM 615527OMIM 616445UMLS C0006845

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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