SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Disorder of organic acid metabolism  116021002

Disorder of amino acid metabolism  44779003

Disorder of amino acid and organic acid metabolism  237911005

Disturbance of tyrosine metabolism   37200009

SNOMED CT code


SNOMED code37200009
nameDisturbance of tyrosine metabolism
statusactive
date introduced2002-01-31
fully specified name(s)Disorder of tyrosine metabolism (disorder)
synonyms
  • Disorder of tyrosine metabolism
  • Disturbance of tyrosine metabolism
parentsDisorder of amino acid and organic acid metabolism   237911005
children
  • 4-Hydroxyphenylpyruvate dioxygenase deficiency   413356003
  • Alcaptonuria   367388008  removed: 2004-07-31
  • Disorder of catecholamine synthesis   237921002
  • Hepatic tyrosine aminotransferase deficiency   360410009
  • Homogentisate 1,2-dioxygenase deficiency   360378009
  • Homogentisic acid defect   237915001  removed: 2004-07-31
  • Hypertyrosinemia   56595005
  • Hypopigmentation-immunodeficiency disease   37548006
  • Tyrosinase-negative oculocutaneous albinism   6483008
  • Tyrosinemia   190694001
  • Tyrosinosis   57414003
  • Tyrosinuria   123967008
  • Woolf's syndrome   74320008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of amino acid metabolism   44779003
            Disorder of amino acid and organic acid metabolism   237911005
              Disturbance of tyrosine metabolism   37200009

ancestors
sorted most to least specific
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