Elevated long chain fatty acids

Symptom Information:

Symptom ID: HPO:0003455
Synonyms:
Increased serum long-chain fatty acids [HPO:0003455]
Elevated long chain fatty acids [OMIM:Elevated long chain fatty acids]
Increased serum long-chain fatty acids [OMIM:Increased serum long-chain fatty acids]
Quality:
Cross references:
OMIM: "Elevated long chain fatty acids" [OMIM:Elevated long chain fatty acids]
OMIM: "Increased serum long-chain fatty acids" [OMIM:Increased serum long-chain fatty acids]
Is a (Direct Parents):
HPO         Abnormality of long-chain fatty-acid metabolism
HPO         Elevated serum long-chain fatty acids
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:
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)