X-linked dominant erythropoietic protoporphyria   1197360001

SNOMED CT code


SNOMED code1197360001
nameX-linked dominant erythropoietic protoporphyria
statusactive
date introduced2022-02-28
fully specified name(s)X-linked dominant erythropoietic protoporphyria (disorder)
synonymsX-linked dominant erythropoietic protoporphyria
attributes - group1
OccurrenceCongenital   255399007
parents
  • X-linked dominant hereditary disease   1162984000
  • Erythropoietic protoporphyria   51022005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked dominant hereditary disease   1162984000
                X-linked dominant erythropoietic protoporphyria   1197360001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital porphyria   190913009
          Erythropoietic protoporphyria   51022005
            X-linked dominant erythropoietic protoporphyria   1197360001

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.