Abnormal pattern of respiration
Symptom Information:
Symptom ID: | HPO:0002793 | ||||||
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) Functional respiratory abnormality(HPO:0002795) Abnormal pattern of respiration(HPO:0002793) MedDRA: |
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Database Frequency: | 26 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Adult pulmonary Langerhans cell histiocytosis | (Orphanet:99874) |
Atypical Rett syndrome | (Orphanet:3095) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Encephalopathy due to sulfite oxidase deficiency | (Orphanet:833) |
Gaucher disease type 2 | (Orphanet:77260) |
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type | (Orphanet:79399) |
Haddad syndrome | (Orphanet:99803) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Idiopathic acute eosinophilic pneumonia | (Orphanet:724) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Leigh syndrome | (Orphanet:506) |
Patent arterial duct | (Orphanet:706) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Pycnodysostosis | (Orphanet:763) |
Pyruvate dehydrogenase deficiency | (Orphanet:765) |
Rett syndrome | (Orphanet:778) |
Scleroderma | (Orphanet:801) |
Spontaneous periodic hypothermia | (Orphanet:29822) |
Sporadic Leigh syndrome | (Orphanet:255199) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |
Takayasu arteritis | (Orphanet:3287) |