SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal recessive hereditary disorder  85995004

21-hydroxylase deficiency   698855007

SNOMED CT code


SNOMED code698855007
name21-hydroxylase deficiency
statusremoved
date introduced2014-01-31
date removed2017-01-31
fully specified name(s)21-hydroxylase deficiency (disorder)
synonyms
  • CYP21 deficiency
  • 21-hydroxylase deficiency
parentsAutosomal recessive hereditary disorder   85995004
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 recessive hereditary disorder   85995004
              21-hydroxylase deficiency   698855007  removed: 2017-01-31

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

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