Diagnosis Code: G71.09

Short Description: Other specified muscular dystrophies

Long Description: Other specified muscular dystrophies

The code G71.09 is VALID for claim submission

Code Classification:

• Diseases of the nervous system (G00–G99)
  • Diseases of myoneural junction and muscle (G70-G73)
    • Primary disorders of muscles (G71)
      • G71.09 Other specified muscular dystrophies

Code Version: 2022 ICD-10-CM

Synonyms

• Adenylosuccinate synthetase-like 1-related distal myopathy
• Adult onset autosomal recessive muscular dystrophy with normal dystrophin
• Adult-onset distal myopathy due to valosin containing protein mutation
• Autosomal dominant Emery-Dreifuss muscular dystrophy
• Autosomal dominant muscular dystrophy not predominantly limb girdle
• Autosomal dominant muscular dystrophy with gene located at 5q31
• Autosomal dominant muscular dystrophy with gene located at 5q31
• Autosomal dominant muscular dystrophy with limb girdle distribution
• Autosomal dominant muscular dystrophy with limb girdle distribution
• Autosomal recessive Emery-Dreifuss muscular dystrophy
• Autosomal recessive muscular dystrophy not predominantly limb girdle
• Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
• Benign congenital muscular dystrophy with finger flexion contractures
• Benign scapuloperoneal muscular dystrophy
• Caveolin 3 related distal myopathy
• Combined malformation of central nervous system and skeletal muscle
• Combined malformation of central nervous system and skeletal muscle
• Combined malformation of central nervous system and skeletal muscle
• Combined malformation of central nervous system and skeletal muscle
• Congenital hereditary muscular dystrophy
• Congenital muscular dystrophy due to LMNA mutation
• Congenital muscular dystrophy Paradas type
• Congenital muscular dystrophy type 1A
• Congenital muscular dystrophy type 1B
• Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation
• Congenital muscular dystrophy type 1D large gene mutation
• Congenital muscular dystrophy with arthrogryposis multiplex congenita
• Congenital muscular dystrophy with cerebellar involvement
• Congenital muscular dystrophy with hyperlaxity
• Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
• Congenital muscular dystrophy with integrin alpha-7 deficiency
• Congenital muscular dystrophy with intellectual disability
• Congenital muscular dystrophy with intellectual disability and severe epilepsy
• Congenital muscular dystrophy without intellectual disability
• Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
• Distal anoctaminopathy
• Distal muscular dystrophy with juvenile onset
• Distal muscular dystrophy, Miyoshi type
• Distal myopathy 2
• Distal myopathy Welander type
• Distal myopathy with anterior tibial onset
• Distal myopathy with posterior leg and anterior hand involvement
• Distal nebulin myopathy
• Early onset myopathy with fatal cardiomyopathy
• Eichsfeld type congenital muscular dystrophy
• Emery-Dreifuss muscular dystrophy
• Enlargement of skeletal muscle
• Enlargement of skeletal muscle
• Finding of appearance of skeletal muscle
• Finding of appearance of skeletal muscle
• Finding of size of skeletal muscle
• Finding of size of skeletal muscle
• Finnish upper limb onset distal myopathy
• Fukuyama congenital muscular dystrophy
• Hereditary progressive muscular dystrophy
• Hoffman syndrome
• Hutterite type of muscular dystrophy
• Infantile and/or juvenile cataract
• Infantile cataract
• Intermediate X-linked muscular dystrophy
• KLHL9-related early-onset distal myopathy
• Laing early-onset distal myopathy
• Late onset proximal muscular dystrophy with dysarthria
• Late-onset distal myopathy Markesbery Griggs type
• Manifesting female carrier of X-linked muscular dystrophy
• Megaconial congenital muscular dystrophy
• Merosin deficient congenital muscular dystrophy
• Muscle eye brain disease with bilateral multicystic leukodystrophy
• Muscle-eye-brain disease, congenital muscular dystrophy
• Muscular dystrophy Selcen type
• Neurogenic scapuloperoneal syndrome Kaeser type
• Nonsenile cataract
• Oculogastrointestinal muscular dystrophy
• Oculopharyngeal muscular dystrophy
• Oculopharyngodistal myopathy
• Pharyngeal paresis
• POGLUT1-related limb girdle muscular dystrophy R21
• Progressive scapulohumeroperoneal distal myopathy
• Pseudohypertrophy of muscle
• Pseudohypertrophy of muscle
• Reunion-Indiana Amish type muscular dystrophy
• Scapuloperoneal muscular dystrophy
• Scapuloperoneal muscular dystrophy
• Severe childhood autosomal recessive muscular dystrophy
• Severe scapuloperoneal muscular dystrophy with cardiomyopathy
• Type 2 lissencephaly
• Walker-Warburg congenital muscular dystrophy
• Weakness of vocal cord
• Western type of congenital muscular dystrophy
• X-linked Emery-Dreifuss muscular dystrophy
• X-linked muscular dystrophy with abnormal dystrophin
• X-linked muscular dystrophy with abnormal dystrophin
• X-linked muscular dystrophy with limb girdle distribution
• X-linked muscular dystrophy with limb girdle distribution
• X-linked muscular dystrophy with limb girdle distribution
• X-linked scapuloperoneal muscular dystrophy

References to Index of Diseases and Injuries

The code G71.09 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]
  • Congenital muscular dystrophy NOS
  • Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiber
  • Distal muscular dystrophy
  • Ocular muscular dystrophy
  • Oculopharyngeal muscular dystrophy
  • Scapuloperoneal muscular dystrophy

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This page was last updated on: 10/1/2023

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