Apneic episodes in infancy
Symptom Information:
Symptom ID: | HPO:0005949 | ||
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) Abnormal pattern of respiration(HPO:0002793) Apnea(HPO:0002104) Apneic episodes in infancy(HPO:0005949) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
2-methylbutyryl-CoA dehydrogenase deficiency | (Orphanet:79157) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Potassium-aggravated myotonia | (Orphanet:612) |
Pyruvate dehydrogenase E1-alpha deficiency | (Orphanet:79243) |
SUDDEN INFANT DEATH SYNDROME | (OMIM:272120) |