Bronchiectasis
Symptom Information:
| Symptom ID: | HPO:0002110 | ||||||||
| Synonyms: |
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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 the upper respiratory tract(HPO:0002087) Abnormality of the tracheobronchial system(HPO:0005607) Abnormality of the bronchi(HPO:0002109) Bronchiectasis(HPO:0002110) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Bronchial disorders (excl neoplasms)(MedDRA:10006436) Bronchial conditions NEC(MedDRA:10006429) Bronchiectasis(HPO:0002110) |
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| Database Frequency: | 73 / 7739 | ||||||||
| Resource: |
All diseases associated with this symptom:
| AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE | (OMIM:601495) |
| ATAXIA-TELANGIECTASIA | (OMIM:208900) |
| Acute interstitial pneumonia | (Orphanet:79126) |
| Allergic bronchopulmonary aspergillosis | (Orphanet:1164) |
| Ataxia-telangiectasia | (Orphanet:100) |
| Autosomal agammaglobulinemia | (Orphanet:33110) |
| BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1 | (OMIM:211400) |
| BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2 | (OMIM:613021) |
| BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3 | (OMIM:613071) |
| Bloom syndrome | (Orphanet:125) |
| Bronchiolitis obliterans with obstructive pulmonary disease | (Orphanet:1303) |
| CILIARY DYSKINESIA, PRIMARY, 1 | (OMIM:244400) |
| CILIARY DYSKINESIA, PRIMARY, 11 | (OMIM:612649) |
| CILIARY DYSKINESIA, PRIMARY, 12 | (OMIM:612650) |
| CILIARY DYSKINESIA, PRIMARY, 13 | (OMIM:613193) |
| CILIARY DYSKINESIA, PRIMARY, 14 | (OMIM:613807) |
| CILIARY DYSKINESIA, PRIMARY, 15 | (OMIM:613808) |
| CILIARY DYSKINESIA, PRIMARY, 16 | (OMIM:614017) |
| CILIARY DYSKINESIA, PRIMARY, 17 | (OMIM:614679) |
| CILIARY DYSKINESIA, PRIMARY, 19 | (OMIM:614935) |
| CILIARY DYSKINESIA, PRIMARY, 2 | (OMIM:606763) |
| CILIARY DYSKINESIA, PRIMARY, 20 | (OMIM:615067) |
| CILIARY DYSKINESIA, PRIMARY, 21 | (OMIM:615294) |
| CILIARY DYSKINESIA, PRIMARY, 22 | (OMIM:615444) |
| CILIARY DYSKINESIA, PRIMARY, 23 | (OMIM:615451) |
| CILIARY DYSKINESIA, PRIMARY, 24 | (OMIM:615481) |
| CILIARY DYSKINESIA, PRIMARY, 25 | (OMIM:615482) |
| CILIARY DYSKINESIA, PRIMARY, 26 | (OMIM:615500) |
| CILIARY DYSKINESIA, PRIMARY, 27 | (OMIM:615504) |
| CILIARY DYSKINESIA, PRIMARY, 28 | (OMIM:615505) |
| CILIARY DYSKINESIA, PRIMARY, 29 | (OMIM:615872) |
| CILIARY DYSKINESIA, PRIMARY, 30 | (OMIM:616037) |
| CILIARY DYSKINESIA, PRIMARY, 5 | (OMIM:608647) |
| CILIARY DYSKINESIA, PRIMARY, 7 | (OMIM:611884) |
| CILIARY DYSKINESIA, PRIMARY, 9 | (OMIM:612444) |
| Combined pulmonary fibrosis-emphysema syndrome | (Orphanet:300564) |
| Common variable immunodeficiency | (Orphanet:1572) |
| Cryptogenic organizing pneumonia | (Orphanet:1302) |
| Cryptosporidiosis - chronic cholangitis - liver disease | (Orphanet:357329) |
| Cutis laxa | (Orphanet:209) |
| Cystic fibrosis | (Orphanet:586) |
| Desquamative interstitial pneumonia | (Orphanet:98852) |
| Diffuse panbronchiolitis | (Orphanet:171700) |
| Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
| Good syndrome | (Orphanet:169105) |
| Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
| Hyper-IgM syndrome type 4 | (Orphanet:101091) |
| ICF syndrome | (Orphanet:2268) |
| IMMUNODEFICIENCY 14 | (OMIM:615513) |
| IMMUNODEFICIENCY 23 | (OMIM:615816) |
| IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
| IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
| IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
| IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 | (OMIM:242860) |
| Idiopathic bronchiectasis | (Orphanet:60033) |
| Idiopathic pulmonary fibrosis | (Orphanet:2032) |
| Immunodeficiency by defective expression of HLA class 1 | (Orphanet:34592) |
| MACS syndrome | (Orphanet:217335) |
| MUCUS INSPISSATION OF RESPIRATORY TRACT | (OMIM:253240) |
| MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
| Nephronophthisis 12 | (OMIM:613820) |
| Nephronophthisis 15 | (OMIM:614845) |
| Nijmegen breakage syndrome | (Orphanet:647) |
| Non-specific interstitial pneumonia | (Orphanet:91364) |
| Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
| Rothmund-Thomson syndrome | (Orphanet:2909) |
| Sarcoidosis | (Orphanet:797) |
| Susceptibility to chronic infection by Epstein-Barr virus | (Orphanet:2566) |
| Susceptibility to respiratory infections associated with CD8alpha chain mutation | (Orphanet:169085) |
| Thymic aplasia | (Orphanet:83471) |
| Tracheobronchomegaly | (Orphanet:3347) |
| Yellow nail syndrome | (Orphanet:662) |
| Young syndrome | (Orphanet:3471) |