Reye syndrome-like episodes
Symptom Information:
Symptom ID: | HPO:0006582 | ||
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 abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Reye syndrome-like episodes(HPO:0006582) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Carnitine uptake deficiency | (Orphanet:158) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Navajo neurohepatopathy | (Orphanet:255229) |