Recurrent pneumonia

Symptom Information:

Symptom ID: HPO:0006532
Synonyms:
Multiple pulmonary infections [HPO:0006532]
Pneumonia, recurrent [HPO:0006532]
Pneumonia, recurrent episodes [HPO:0006532]
Pulmonary infection [HPO:0006532]
Pulmonary infections [HPO:0006532]
pulmonary infections, recurrent [HPO:0006532]
Recurrent pulmonary infections [HPO:0006532]
Multiple pulmonary infections [OMIM:Multiple pulmonary infections]
Pneumonia, recurrent [OMIM:Pneumonia, recurrent]
Pneumonia, recurrent episodes [OMIM:Pneumonia, recurrent episodes]
Pulmonary infections [OMIM:Pulmonary infections]
Pulmonary infections, recurrent [OMIM:Pulmonary infections, recurrent]
Recurrent pneumonia [OMIM:Recurrent pneumonia]
Recurrent pulmonary infections [OMIM:Recurrent pulmonary infections]
Pneumonia, recurrent (reported in 1 family) [OMIM:Pneumonia, recurrent (reported in 1 family)]
Recurrent pneumonia (in some patients) [OMIM:Recurrent pneumonia (in some patients)]
Recurrent pulmonary infection [OMIM:Recurrent pulmonary infection]
Quality:
Cross references:
OMIM: "Multiple pulmonary infections" [OMIM:Multiple pulmonary infections]
OMIM: "Pneumonia, recurrent" [OMIM:Pneumonia, recurrent]
OMIM: "Pneumonia, recurrent episodes" [OMIM:Pneumonia, recurrent episodes]
OMIM: "Pulmonary infections" [OMIM:Pulmonary infections]
OMIM: "Pulmonary infections, recurrent" [OMIM:Pulmonary infections, recurrent]
OMIM: "Recurrent pneumonia" [OMIM:Recurrent pneumonia]
OMIM: "Recurrent pulmonary infections" [OMIM:Recurrent pulmonary infections]
OMIM: "Pneumonia, recurrent (reported in 1 family)" [OMIM:Pneumonia, recurrent (reported in 1 family)]
OMIM: "Recurrent pneumonia (in some patients)" [OMIM:Recurrent pneumonia (in some patients)]
OMIM: "Recurrent pulmonary infection" [OMIM:Recurrent pulmonary infection]
Is a (Direct Parents):
HPO         Recurrent lower respiratory tract infections
HPO         Pneumonia
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)
                      Recurrent pneumonia(HPO:0006532)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Respiratory tract infection(HPO:0011947)
                   Pneumonia(HPO:0002090)
                      Recurrent pneumonia(HPO:0006532)
                   Recurrent respiratory infections(HPO:0002205)
                      Recurrent lower respiratory tract infections(HPO:0002783)
                         Recurrent pneumonia(HPO:0006532)
MedDRA:
Database Frequency: 48 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE (OMIM:601495)
AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE (OMIM:613500)
AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE (OMIM:613502)
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE (OMIM:612692)
Aicardi syndrome (Orphanet:50)
Alström syndrome (Orphanet:64)
Autosomal agammaglobulinemia (Orphanet:33110)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
Bardet-Biedl syndrome 16 (OMIM:615993)
CILIARY DYSKINESIA, PRIMARY, 20 (OMIM:615067)
Congenital muscular dystrophy type 1A (Orphanet:258)
Cranioectodermal dysplasia 4 (OMIM:614378)
Cystic fibrosis (Orphanet:586)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
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)
Hallermann-Streiff syndrome (Orphanet:2108)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
IMMUNODEFICIENCY WITH DEFECTIVE T-CELL RESPONSE TO INTERLEUKIN 1 (OMIM:243110)
IMMUNODEFICIENCY, COMMON VARIABLE, 1 (OMIM:607594)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
IMMUNODEFICIENCY, COMMON VARIABLE, 4 (OMIM:613494)
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2 (OMIM:616069)
Leprechaunism (Orphanet:508)
MASP2 DEFICIENCY (OMIM:613791)
MEIER-GORLIN SYNDROME 3 (OMIM:613803)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 2 (Orphanet:580)
Nijmegen breakage syndrome (Orphanet:647)
Obesity due to congenital leptin deficiency (Orphanet:66628)
Osteopetrosis - hypogammaglobulinemia (Orphanet:178389)
Otospondylomegaepiphyseal dysplasia (Orphanet:1427)
Poikiloderma with neutropenia (Orphanet:221046)
Prolidase deficiency (Orphanet:742)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
ROWLEY-ROSENBERG SYNDROME (OMIM:268500)
Roifman syndrome (Orphanet:353298)
Scheie syndrome (Orphanet:93474)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification (Orphanet:93358)
TRIMETHYLAMINURIA (OMIM:602079)
Thymic aplasia (Orphanet:83471)
Tracheobronchopathia osteochondroplastica (Orphanet:3348)
X-linked reticulate pigmentary disorder with systemic manifestations (Orphanet:85453)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)