SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Metabolic disease  75934005

Hereditary metabolic disease  1821000146108

Hereditary xanthinuria  54627004

Combined molybdoflavoprotein enzyme deficiency  29692004

Molybdenum cofactor deficiency complementation group B   1003368009

SNOMED CT code


SNOMED code1003368009
nameMolybdenum cofactor deficiency complementation group B
statusactive
date introduced2021-01-31
fully specified name(s)Molybdenum cofactor deficiency complementation group B (disorder)
synonymsMolybdenum cofactor deficiency complementation group B
attributes - group1
Finding siteKidney structure   64033007
parentsCombined molybdoflavoprotein enzyme deficiency   29692004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Hereditary metabolic disease   1821000146108
          Hereditary xanthinuria   54627004
            Combined molybdoflavoprotein enzyme deficiency   29692004
              Molybdenum cofactor deficiency complementation group B   1003368009

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