Propionyl-CoA carboxylase deficiency

Symptom Information:

Symptom ID: HPO:0003353
Synonyms:
Propionyl-CoA carboxylase deficiency [OMIM:Propionyl-CoA carboxylase deficiency]
Quality:
Cross references:
OMIM: "Propionyl-CoA carboxylase deficiency" [OMIM:Propionyl-CoA carboxylase deficiency]
Is a (Direct Parents):
HPO         Abnormality of amino acid metabolism
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:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY (OMIM:210210)
Propionic acidemia (Orphanet:35)