Propionyl-CoA carboxylase deficiency
Symptom Information:
Symptom ID: | HPO:0003353 | ||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of carboxylic acid metabolism(HPO:0004354) Abnormality of amino acid metabolism(HPO:0004337) Propionyl-CoA carboxylase deficiency(HPO:0003353) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY | (OMIM:210210) |
Propionic acidemia | (Orphanet:35) |