Respiratory tract infection
Symptom Information:
Symptom ID: | HPO:0011947 | ||||||||
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) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Respiratory tract infection(HPO:0011947) |
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Database Frequency: | 28 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Alström syndrome | (Orphanet:64) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Bardet-Biedl syndrome 16 | (OMIM:615993) |
Bloom syndrome | (Orphanet:125) |
CADASIL | (Orphanet:136) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
IMMUNODEFICIENCY 15 | (OMIM:615592) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | (Orphanet:352563) |
Leprechaunism | (Orphanet:508) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Microcephalic primordial dwarfism, Toriello type | (Orphanet:2643) |
Mulibrey nanism | (Orphanet:2576) |
Niemann-Pick disease type A | (Orphanet:77292) |
Niemann-Pick disease type B | (Orphanet:77293) |
Niemann-Pick disease type E | (Orphanet:99022) |
PEROXISOME BIOGENESIS DISORDER 11B | (OMIM:614885) |
Primary Fanconi syndrome | (Orphanet:3337) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE | (OMIM:277300) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |