Respiratory arrest
Symptom Information:
Symptom ID: | HPO:0005943 | ||||
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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) Respiratory insufficiency(HPO:0002093) Respiratory arrest(HPO:0005943) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Respiratory arrest(HPO:0005943) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Respiratory disorders NEC(MedDRA:10038716) Breathing abnormalities(MedDRA:10006334) Respiratory arrest(HPO:0005943) |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Citrullinemia type I | (Orphanet:247525) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Pyruvate dehydrogenase E1-beta deficiency | (Orphanet:255138) |