Breathing dysregulation
Symptom Information:
Symptom ID: | HPO:0005957 | ||
Synonyms: |
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Quality: | |||
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) Breathing dysregulation(HPO:0005957) MedDRA: |
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Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Joubert syndrome 6 | (OMIM:610688) |
Leigh syndrome | (Orphanet:506) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |