Decreased plasma total carnitine
Symptom Information:
Symptom ID: | HPO:0011936 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |