Acute encephalopathy
Symptom Information:
Symptom ID: | HPO:0006846 | ||
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 nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Encephalopathy(HPO:0001298) Acute encephalopathy(HPO:0006846) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Neurological conditions associated with aminoacylase 1 deficiency | (Orphanet:137754) |
Propionic acidemia | (Orphanet:35) |