Recurrent fungal infections
Symptom Information:
Symptom ID: | HPO:0002841 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Recurrent infections(HPO:0002719) Recurrent fungal infections(HPO:0002841) MedDRA: |
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Database Frequency: | 16 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Autosomal recessive hyper-IgE syndrome | (Orphanet:169446) |
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency | (Orphanet:331226) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Combined immunodeficiency due to STK4 deficiency | (Orphanet:314689) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE | (OMIM:233690) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE I | (OMIM:233700) |
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE II | (OMIM:233710) |
GRANULOMATOUS DISEASE, CHRONIC, X-LINKED | (OMIM:306400) |
Immunodeficiency by defective expression of HLA class 2 | (Orphanet:572) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Monocytopenia with susceptibility to infections | (Orphanet:228423) |
Omenn syndrome | (Orphanet:39041) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
T-B+ severe combined immunodeficiency due to gamma chain deficiency | (Orphanet:276) |
Vici syndrome | (Orphanet:1493) |