Recurrent viral infections
Symptom Information:
Symptom ID: | HPO:0004429 | ||
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 viral infections(HPO:0004429) MedDRA: |
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Database Frequency: | 20 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive hyper-IgE syndrome | (Orphanet:169446) |
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency | (Orphanet:331226) |
CANDIDIASIS, FAMILIAL, 1 | (OMIM:114580) |
COXSACKIEVIRUS B3 SUSCEPTIBILITY | (OMIM:120050) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Combined immunodeficiency due to DOCK8 deficiency | (Orphanet:217390) |
Combined immunodeficiency due to STK4 deficiency | (Orphanet:314689) |
IMMUNE DEFICIENCY DISEASE | (OMIM:242850) |
IMMUNODEFICIENCY 12 | (OMIM:615468) |
Immunodeficiency by defective expression of HLA class 2 | (Orphanet:572) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Immunodeficiency with natural-killer cell deficiency | (Orphanet:75391) |
MYELOLYMPHATIC INSUFFICIENCY | (OMIM:310350) |
Monocytopenia with susceptibility to infections | (Orphanet:228423) |
Omenn syndrome | (Orphanet:39041) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Susceptibility to respiratory infections associated with CD8alpha chain mutation | (Orphanet:169085) |
Vici syndrome | (Orphanet:1493) |
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia | (Orphanet:317476) |