Decreased plasma free carnitine
Symptom Information:
Symptom ID: | HPO:0008315 | ||
Synonyms: |
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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 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 free carnitine(HPO:0008315) 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 free carnitine(HPO:0008315) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
2,4-@DIENOYL-CoA REDUCTASE DEFICIENCY | (OMIM:616034) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |