SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal recessive hereditary disorder  85995004

Methylmalonyl-CoA mutase deficiency   28292003

SNOMED CT code


SNOMED code28292003
nameMethylmalonyl-CoA mutase deficiency
statusremoved
date introduced2002-01-31
date removed2004-07-31
fully specified name(s)Methylmalonyl-CoA mutase deficiency (disorder)
synonyms
  • Vitamin B12 non-responsive methylmalonic acidaemia
  • Vitamin B12 non-responsive methylmalonic acidemia
  • Methylmalonyl-CoA mutase apoenzyme deficiency
  • Methylmalonyl-CoA mutase 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
              Methylmalonyl-CoA mutase deficiency   28292003  removed: 2004-07-31

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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