Erythropoietic uroporphyria associated with myeloid malignancy   783615009

SNOMED CT code


SNOMED code783615009
nameErythropoietic uroporphyria associated with myeloid malignancy
statusactive
date introduced2019-07-31
fully specified name(s)Erythropoietic uroporphyria associated with myeloid malignancy (disorder)
synonymsErythropoietic uroporphyria associated with myeloid malignancy
attributes - group1
Associated morphologyMyelodysplastic neoplasm   128623006
parents
  • Uroporphyrinuria   123964001
  • Malignant tumor of lymphoid hemopoietic and related tissue   269475001
  • Disorder of hematopoietic morphology   414026006
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of porphyrin metabolism   29094004
          Porphyria   418470004
            Uroporphyrinuria   123964001
              Erythropoietic uroporphyria associated with myeloid malignancy   783615009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Neoplasm and/or hamartoma   399981008
        Neoplastic disease   55342001
          Malignant tumor   363346000
            Malignant tumor of lymphoid hemopoietic and related tissue   269475001
              Erythropoietic uroporphyria associated with myeloid malignancy   783615009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of hematopoietic morphology   414026006
        Erythropoietic uroporphyria associated with myeloid malignancy   783615009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Erythropoietic uroporphyria associated with myeloid malignancy   783615009

ancestors
sorted most to least specific
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