Metabolic and genetic disorder affecting the liver   235903001

SNOMED CT code


SNOMED code235903001
nameMetabolic and genetic disorder affecting the liver
statusactive
date introduced2002-01-31
fully specified name(s)Metabolic and genetic disorder affecting the liver (disorder)
synonymsMetabolic and genetic disorder affecting the liver
attributes - group1
Finding siteLiver structure   10200004
parents
children
  • Alpha-1-antitrypsin deficiency   30188007
  • Antichymotrypsin deficiency-alpha-1   235909002
  • Congenital cystic disease of liver   72925005
  • Contiguous ABCD1 DXS1357E deletion syndrome   773415005
  • Dubin-Johnson syndrome   44553005
  • Ferro-cerebro-cutaneous syndrome   774151000
  • FTH1-related iron overload   1230310007
  • Glycogen storage disease, hepatic form   6075009
  • Hemochromatosis   86781004  removed: 2003-07-31
  • Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1   764962002
  • Hyperbilirubinemia   235904007  removed: 2002-07-31
  • Liver calculus   297288000
  • Mitochondrial DNA depletion syndrome hepatocerebrorenal form   782771007
  • Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency   783734000
  • Mucopolysaccharidosis, MPS-II   70737009
  • Navajo neurohepatopathy   784346006
  • Progressive intrahepatic cholestasis   74162007
  • Steroid dehydrogenase deficiency and dental anomaly syndrome   723583009
  • Synthetic defect of bile acids   235915002
  • Wilson's disease   88518009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Liver finding   249565005
        Disease of liver   235856003
          Metabolic and genetic disorder affecting the liver   235903001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic and genetic disorder affecting the liver   235903001

ancestors
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