Long chain 3 hydroxyacyl coA dehydrogenase deficiency
Symptom Information:
Symptom ID: | HPO:0100950 | ||||
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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 cell physiology(HPO:0011017) Abnormality of the mitochondrion(HPO:0012103) Abnormality of mitochondrial metabolism(HPO:0003287) Long chain 3 hydroxyacyl coA dehydrogenase deficiency(HPO:0100950) Abnormality of lipid metabolism(HPO:0003119) Abnormality of fatty-acid metabolism(HPO:0004359) Abnormality of long-chain fatty-acid metabolism(HPO:0010964) Long chain 3 hydroxyacyl coA dehydrogenase deficiency(HPO:0100950) MedDRA: |
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Database Frequency: | 1 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |