chronic mucocutaneous candidiasis
MONDO:0015279Mondo
Findings
No curated finding names chronic mucocutaneous candidiasis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Features
31 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Abnormal fingernail morphologyHPOHP:0001231
- Very frequent (80% to 99% of cases)
- Abnormal lip morphologyHPOHP:0000159
- Very frequent (80% to 99% of cases)
- Abnormal nail morphologyHPOHP:0001597
- Very frequent (80% to 99% of cases)
- Abnormal toenail morphologyHPOHP:0008388
- Very frequent (80% to 99% of cases)
- Abnormality of the immune systemHPOHP:0002715
- Very frequent (80% to 99% of cases)
- Abnormality of the mouthHPOHP:0000153
- Very frequent (80% to 99% of cases)
- Abnormality of the skinHPOHP:0000951
- Very frequent (80% to 99% of cases)
- Broad nailHPOHP:0001821
- Very frequent (80% to 99% of cases)
- CheilitisHPOHP:0100825
- Very frequent (80% to 99% of cases)
- ErythemaHPOHP:0010783
- Very frequent (80% to 99% of cases)
- HyperkeratosisHPOHP:0000962
- Very frequent (80% to 99% of cases)
- Recurrent infectionsHPOHP:0002719
- Very frequent (80% to 99% of cases)
Show the remaining 19
- Skin rashHPOHP:0000988
- Very frequent (80% to 99% of cases)
- Skin ulcerHPOHP:0200042
- Very frequent (80% to 99% of cases)
- Abnormal vagina morphologyHPOHP:0000142
- Frequent (30% to 79% of cases)
- DyspareuniaHPOHP:0030016
- Frequent (30% to 79% of cases)
- PapuleHPOHP:0200034
- Frequent (30% to 79% of cases)
- Abnormal dental enamel morphologyHPOHP:0000682
- Occasional (5% to 29% of cases)
Genes
5 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- CLEC7AHGNC:14558
- Supportive · Orphanet · Autosomal dominant · 2021
- IL17FHGNC:16404
- Supportive · Orphanet · Autosomal dominant · 2021
- IL17RAHGNC:5985
- Supportive · Orphanet · Autosomal dominant · 2021
- IL17RCHGNC:18358
- Supportive · Orphanet · Autosomal dominant · 2021
- TRAF3IP2HGNC:1343
- Supportive · Orphanet · Autosomal dominant · 2021
Where it sits
- Narrower terms (12)
- autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
- candidiasis, familial, 1
- candidiasis, familial, 3
- candidiasis, familial, 4
- candidiasis, familial, 6
- candidiasis, familial, 8
- candidiasis, familial, 9
- chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation
- chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation
- chronic mucocutaneous candidiasis due to lymphokine deficiency
- chronic mucocutaneous candidiasis due to monocyte chemotactic disorder
- immunodeficiency 51
Other names
6 names
Resolves to: chronic mucocutaneous candidiasis
- Also called
- CANDFchronic mucocutaneous candidiasis (disease)CMCfamilial candidiasisfamilial chronic mucocutaneous candidiasisfamilial CMC