Elevated long chain fatty acids
Symptom Information:
Symptom ID: | HPO:0003455 | ||||
Synonyms: |
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Cross references: |
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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 long-chain fatty-acid metabolism(HPO:0010964) Elevated long chain fatty acids(HPO:0003455) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 2B | (OMIM:202370) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |
Zellweger syndrome | (Orphanet:912) |