SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Hereditary cancer-predisposing syndrome  699346009

Schöpf-Schulz-Passarge syndrome   700062000

SNOMED CT code


SNOMED code700062000
nameSchöpf-Schulz-Passarge syndrome
statusactive
date introduced2014-01-31
fully specified name(s)Schöpf-Schulz-Passarge syndrome (disorder)
synonymsSchöpf-Schulz-Passarge syndrome
parentsHereditary cancer-predisposing syndrome   699346009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary cancer-predisposing syndrome   699346009
            Schöpf-Schulz-Passarge syndrome   700062000

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.

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