SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital myasthenic syndrome  230672006

Acetylcholine resynthesis deficiency   230671004

SNOMED CT code


SNOMED code230671004
nameAcetylcholine resynthesis deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Acetylcholine resynthesis deficiency (disorder)
synonymsAcetylcholine resynthesis deficiency
attributes - group1
Finding siteNeuromuscular junction   31627007
Pathological processAutoimmune process   263680009
OccurrenceCongenital   255399007
attributes - group2
Finding siteSkeletal muscle structure   127954009
attributes - group3
Pathological processHypersensitivity process   472963003
parents
  • Congenital myasthenic syndrome   230672006
  • Myasthenia gravis, juvenile form   55051001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital myasthenic syndrome   230672006
          Acetylcholine resynthesis deficiency   230671004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Hypersensitivity condition   473010000
      Immune hypersensitivity disorder by mechanism   427439005
        Antibody-mediated activation and inactivation   362985009
          Myasthenia gravis   91637004
            Myasthenia gravis, juvenile form   55051001
              Acetylcholine resynthesis deficiency   230671004

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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