SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Sex-linked hereditary disorder  82852009

X-linked hereditary disease  128430005

X-linked muscular dystrophy with limb girdle distribution  240047005

X-linked limb girdle muscular dystrophy with normal dystrophin  240051007

Hereditary myopathy limited to females   240053005

SNOMED CT code


SNOMED code240053005
nameHereditary myopathy limited to females
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary myopathy limited to females (disorder)
synonymsHereditary myopathy limited to females
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyDystrophy   4720007
Finding siteSkeletal muscle structure   127954009
attributes - group2
Clinical courseProgressive   255314001
parentsX-linked limb girdle muscular dystrophy with normal dystrophin   240051007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked muscular dystrophy with limb girdle distribution   240047005
                X-linked limb girdle muscular dystrophy with normal dystrophin   240051007
                  Hereditary myopathy limited to females   240053005

ancestors
sorted most to least specific
  • X-linked limb girdle muscular dystrophy with normal dystrophin   240051007
  • X-linked muscular dystrophy with limb girdle distribution   240047005
  • Congenital hereditary muscular dystrophy   111501005
  • X-linked hereditary disease   128430005
  • Muscular dystrophy with predominantly proximal limb girdle distribution   240046001
  • Hereditary progressive muscular dystrophy   193225000
  • Sex-linked hereditary disorder   82852009
  • Congenital anomaly of skeletal muscle   89886004
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Muscular dystrophy   73297009
  • Congenital anomaly of muscle AND/OR tendon   79191007
  • Disorder of skeletal muscle   75047002
  • Hereditary disorder by system   363137000
  • Chronic disease of musculoskeletal system   128237006
  • Congenital anomaly of musculoskeletal system   73573004
  • Degenerative disorder of muscle   363058009
  • Degenerative disorder of musculoskeletal system   363059001
  • Hereditary disease   32895009
  • Disorder of muscle   129565002
  • Chronic disease   27624003
  • Congenital malformation   276654001
  • Disorder of soft tissue   19660004
  • Disorder of musculoskeletal system   928000
  • Degenerative disorder   362975008
  • Genetic disease   782964007
  • Muscle finding   106030000
  • Developmental disorder   5294002
  • General finding of soft tissue   248402002
  • Musculoskeletal finding   106028002
  • Disorder of body system   362965005
  • Congenital disease   66091009
  • Disease   64572001
  • Clinical finding   404684003
  • SNOMED CT Concept   138875005
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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