Decreased plasma total carnitine

Symptom Information:

Symptom ID: HPO:0011936
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Decreased plasma carnitine
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of lipid metabolism(HPO:0003119)
             Abnormality of fatty-acid metabolism(HPO:0004359)
                Abnormality of fatty-acid anion metabolism(HPO:0010966)
                   Abnormality of carnitine metabolism(HPO:0010967)
                      Decreased plasma carnitine(HPO:0003234)
                         Decreased plasma total carnitine(HPO:0011936)
          Abnormality of cell physiology(HPO:0011017)
             Abnormality of the mitochondrion(HPO:0012103)
                Abnormality of mitochondrial metabolism(HPO:0003287)
                   Decreased plasma carnitine(HPO:0003234)
                      Decreased plasma total carnitine(HPO:0011936)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)