SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Nemaline myopathy, early onset type  129621001

Typical nemaline myopathy   1197153000

SNOMED CT code


SNOMED code1197153000
nameTypical nemaline myopathy
statusactive
date introduced2022-02-28
fully specified name(s)Typical nemaline myopathy (disorder)
synonymsTypical nemaline myopathy
attributes - group1
OccurrenceCongenital   255399007
Finding siteSkeletal muscle structure   127954009
parents
  • Nemaline myopathy, early onset type   129621001
  • Autosomal hereditary disorder   1899006
  • Hereditary disorder of musculoskeletal system   363212003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Nemaline myopathy, early onset type   129621001
          Typical nemaline myopathy   1197153000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Typical nemaline myopathy   1197153000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Typical nemaline myopathy   1197153000

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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