Protein avoidance
Symptom Information:
Symptom ID: | HPO:0002038 | ||
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) Abdominal symptom(HPO:0011458) Protein avoidance(HPO:0002038) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Citrullinemia type I | (Orphanet:247525) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |