Recurrent lower respiratory tract infections

Symptom Information:

Symptom ID: HPO:0002783
Synonyms:
Chronic lung infections [HPO:0002783]
Lower respiratory tract infections [HPO:0002783]
Recurrent chest infections [HPO:0002783]
Chronic lung infections [OMIM:Chronic lung infections]
Lower respiratory tract infections [OMIM:Lower respiratory tract infections]
Recurrent chest infections [OMIM:Recurrent chest infections]
Lower respiratory tract infection [MedDRA:10024968]
Quality:
Cross references:
OMIM: "Chronic lung infections" [OMIM:Chronic lung infections]
OMIM: "Lower respiratory tract infections" [OMIM:Lower respiratory tract infections]
OMIM: "Recurrent chest infections" [OMIM:Recurrent chest infections]
Is a (Direct Parents):
MedDRA Lower respiratory tract and lung infections
HPO         Recurrent respiratory infections
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 respiratory infections(HPO:0002205)
                   Recurrent lower respiratory tract infections(HPO:0002783)
       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 lower respiratory tract infections(HPO:0002783)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Lower respiratory tract and lung infections(MedDRA:10025101)
          Recurrent lower respiratory tract infections(HPO:0002783)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
FANCONI-LIKE SYNDROME (OMIM:227850)
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES (OMIM:615966)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Immunodeficiency due to ficolin3 deficiency (Orphanet:331190)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)