Respiratory paralysis
Symptom Information:
Symptom ID: | HPO:0002203 | ||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Muscle weakness(HPO:0001324) Weakness of muscles of respiration(HPO:0004347) Respiratory paralysis(HPO:0002203) Abnormality of the respiratory system(HPO:0002086) Functional respiratory abnormality(HPO:0002795) Weakness of muscles of respiration(HPO:0004347) Respiratory paralysis(HPO:0002203) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acute intermittent porphyria | (Orphanet:79276) |
Hereditary coproporphyria | (Orphanet:79273) |
MUSCULAR ATROPHY, MALIGNANT NEUROGENIC | (OMIM:158650) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |