Recurrent pneumonia
Symptom Information:
Symptom ID: | HPO:0006532 | |||||||||||||||||
Synonyms: |
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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 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) Recurrent pneumonia(HPO:0006532) Pneumonia(HPO:0002090) Recurrent pneumonia(HPO:0006532) 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) MedDRA: |
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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) |