Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein   720461006

SNOMED CT code


SNOMED code720461006
nameAcute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
statusactive
date introduced2017-01-31
fully specified name(s)Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein (disorder)
synonymsAcute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein
attributes - group1
Finding siteLiver structure   10200004
OccurrenceInfancy   3658006
attributes - group2
Clinical courseSudden onset AND/OR short duration   424124008
attributes - group3
Due toDisorder of mitochondrial respiratory chain complexes   237986005
parents
  • Acute digestive system disorder   127321000
  • Acute hepatic failure   197270009
  • Digestive system hereditary disorder   363080007
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Acute disease   2704003
        Acute digestive system disorder   127321000
          Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein   720461006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Liver finding   249565005
        Disease of liver   235856003
          Hepatic failure   59927004
            Acute hepatic failure   197270009
              Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein   720461006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein   720461006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein   720461006

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