SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Maternal riboflavin deficiency   773549000

SNOMED CT code


SNOMED code773549000
nameMaternal riboflavin deficiency
statusactive
date introduced2019-01-31
fully specified name(s)Maternal riboflavin deficiency (disorder)
synonymsMaternal riboflavin deficiency
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Maternal riboflavin deficiency   773549000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Nutritional disorder   2492009
        Vitamin disease   7521001
          Disorder of vitamin B   386066000
            Vitamin B deficiency   47903000
              Ariboflavinosis   20307000
                Maternal riboflavin deficiency   773549000

ancestors
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