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 muscular dystrophy with abnormal dystrophin  240048000

Manifesting female carrier of X-linked muscular dystrophy  240050008

Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier   765197008

SNOMED CT code


SNOMED code765197008
nameSymptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
statusactive
date introduced2018-07-31
fully specified name(s)Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder)
synonymsSymptomatic form of muscular dystrophy of Duchenne and Becker in female carrier
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDystrophy   4720007
Finding siteSkeletal muscle structure   127954009
OccurrenceCongenital   255399007
attributes - group2
Clinical courseProgressive   255314001
parentsManifesting female carrier of X-linked muscular dystrophy   240050008
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 muscular dystrophy with abnormal dystrophin   240048000
                  Manifesting female carrier of X-linked muscular dystrophy   240050008
                    Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier   765197008

ancestors
sorted most to least specific
  • Manifesting female carrier of X-linked muscular dystrophy   240050008
  • X-linked muscular dystrophy with abnormal dystrophin   240048000
  • 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
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