Acute hyperammonemia
Symptom Information:
Symptom ID: | HPO:0008281 | ||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of nitrogen compound homeostasis(HPO:0004364) Azotemia(HPO:0002157) Hyperammonemia(HPO:0001987) Acute hyperammonemia(HPO:0008281) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY | (OMIM:210200) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |