Respiratory tract infection

Symptom Information:

Symptom ID: HPO:0011947
Synonyms:
Respiratory infection [HPO:0011947]
Recurrent respiratory infections [Orphanet:33900]
Respiratory infection [OMIM:Respiratory infection]
Repeat respiratory infections [Orphanet:33900]
Respiratory infections [OMIM:Respiratory infections]
Respiratory tract infections [MedDRA:10024970]
Respiratory tract infection [MedDRA:10062352]
Quality:
Cross references:
HPO:0002205 "Recurrent respiratory infections" [Orphanet:33900]
Orphanet:33900 "Repeat respiratory infections" [Orphanet:33900]
OMIM: "Respiratory infection" [OMIM:Respiratory infection]
OMIM: "Respiratory infections" [OMIM:Respiratory infections]
Is a (Direct Parents):
HPO         Abnormality of lung morphology
MedDRA Respiratory tract infections NEC
Orphanet Abnormality of the respiratory system
MedDRA Respiratory, thoracic and mediastinal disorders
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)
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)