Recurrent sinopulmonary infections

Symptom Information:

Symptom ID: HPO:0005425
Synonyms:
Chronic sinopulmonary infection [HPO:0005425]
Chronic sinopulmonary infection [OMIM:Chronic sinopulmonary infection]
Recurrent sinopulmonary infections [OMIM:Recurrent sinopulmonary infections]
Sinopulmonary infections, recurrent [OMIM:Sinopulmonary infections, recurrent]
Quality:
Cross references:
OMIM: "Chronic sinopulmonary infection" [OMIM:Chronic sinopulmonary infection]
OMIM: "Recurrent sinopulmonary infections" [OMIM:Recurrent sinopulmonary infections]
OMIM: "Sinopulmonary infections, recurrent" [OMIM:Sinopulmonary infections, recurrent]
Is a (Direct Parents):
HPO         Recurrent respiratory infections
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Respiratory tract infection(HPO:0011947)
                   Recurrent respiratory infections(HPO:0002205)
                      Recurrent sinopulmonary infections(HPO:0005425)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent respiratory infections(HPO:0002205)
                   Recurrent sinopulmonary infections(HPO:0005425)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune lymphoproliferative syndrome with recurrent infections (Orphanet:275517)
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:324530)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive hyper-IgE syndrome (Orphanet:169446)
CILIARY DYSKINESIA WITH TRANSPOSITION OF CILIARY MICROTUBULES (OMIM:215520)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
IMMUNODEFICIENCY 14 (OMIM:615513)
IMMUNOGLOBULIN A DEFICIENCY 2 (OMIM:609529)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Young syndrome (Orphanet:3471)