SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Autosomal dominant deficiency of plasminogen   95842004

SNOMED CT code


SNOMED code95842004
nameAutosomal dominant deficiency of plasminogen
statusactive
date introduced2002-01-31
fully specified name(s)Autosomal dominant deficiency of plasminogen (disorder)
synonyms
  • Autosomal dominant deficiency of plasminogen
  • Autosomal dominant deficiency of profibrinolysin
attributes - group1
InterpretsHemostatic function   74848003
Has interpretationAbnormal   263654008
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary hypoplasminogenemia   95841006
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
              Autosomal dominant deficiency of plasminogen   95842004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary hypoplasminogenemia   95841006
            Autosomal dominant deficiency of plasminogen   95842004

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.