G71.09
BillableOther specified muscular dystrophies
Other specified muscular dystrophies
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 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
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- arthrogryposis multiplex congenita (Q74.3)
- metabolic disorders (E70-E88)
- myositis (M60.-)
Also Known As / Clinical Terms
SNOMED CT
- Oculopharyngeal dystrophy77097004
- Oculopharyngeal muscular dystrophy77097004
- Congenital hereditary muscular dystrophy111501005
- Fukuyama congenital muscular dystrophy111502003
- Fukuyama muscular dystrophy111502003
- Merosin deficient congenital muscular dystrophy111503008
- HARD (hydrocephalus, agyria, retinal dysplasia) syndrome111504002
- Hydrocephalus, agyria and retinal dysplasia111504002
- Walker Warburg syndrome111504002
- Walker-Warburg congenital muscular dystrophy111504002
- COD-MD - Cerebro-oculo-dysgenesis-muscular dystrophy syndrome111505001
- Cerebro-oculo-dysgenesis-muscular dystrophy syndrome111505001
- Muscle-eye-brain disease, congenital muscular dystrophy111505001
- Distal muscular dystrophy, Miyoshi type111506000
- Benign scapuloperoneal muscular dystrophy with early contractures111508004
- EMD - Emery-Dreifuss muscular dystrophy111508004
- Emery-Dreifuss muscular dystrophy111508004
- Pharyngeal paresis129567005
- Pharyngeal weakness129567005
- Scapuloperoneal muscular dystrophy129620000
- Hereditary progressive muscular dystrophy193225000
- Distal muscular dystrophy with juvenile onset193230001
- X-linked muscular dystrophy with limb girdle distribution240047005
- Meryon muscular dystrophy240048000
- X-linked muscular dystrophy with abnormal dystrophin240048000
- Xp21-linked muscular dystrophy240048000
- Intermediate X-linked muscular dystrophy240049008
- Manifesting female carrier of X-linked muscular dystrophy240050008
- Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein240055003
- Reunion-Indiana Amish type muscular dystrophy240058001
- Western type of congenital muscular dystrophy240060004
- Congenital muscular dystrophy with arthrogryposis multiplex congenita240061000
- Eichsfeld type congenital muscular dystrophy240063002
- Rigid spine syndrome240063002
- Hutterite type of muscular dystrophy240064008
- Adult onset autosomal recessive muscular dystrophy with normal dystrophin240065009
- Autosomal dominant muscular dystrophy with limb girdle distribution240067001
- Autosomal dominant muscular dystrophy with gene located at 5q31240068006
- Gilchrist type muscular dystrophy240069003
- Late onset proximal muscular dystrophy with dysarthria240069003
- Autosomal recessive muscular dystrophy not predominantly limb girdle240073000
- Autosomal dominant muscular dystrophy not predominantly limb girdle240075007
- Benign scapuloperoneal muscular dystrophy240076008
- Severe scapuloperoneal muscular dystrophy with cardiomyopathy240077004
- Benign congenital muscular dystrophy with finger flexion contractures240078009
- Pseudohypertrophy of muscle249830001
- Type 2 lissencephaly253149002
- SCARMD - Severe childhood autosomal recessive muscular dystrophy277373000
- Severe childhood autosomal recessive muscular dystrophy277373000
- Combined malformation of central nervous system and skeletal muscle277949001
- Infantile cataract399120006
- Non age related cataract399305009
- Non age-related cataract399305009
- Nonsenile cataract399305009
- Weakness of vocal cord445424004
- Early onset myopathy with fatal cardiomyopathy702343002
- Salih congenital muscular dystrophy702343002
- Salih myopathy702343002
- Distal myopathy 2702383005
- Distal myopathy with vocal cord weakness702383005
- MATR3-related distal myopathy702383005
- Matrin 3 distal myopathy702383005
- Myopathia distalis type 2702383005
- VCPDM - vocal cord and pharyngeal distal myopathy702383005
- Vocal cord and pharyngeal distal myopathy702383005
- Vocal cord and pharyngeal dysfunction with distal myopathy702383005
- CAV3-related distal myopathy711265009
- Caveolin 3 related distal myopathy711265009
- Distal myopathy, Tateyama type711265009
- Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome715429006
- Hoffman syndrome716338001
- Kocher Debre Semelaigne syndrome716338001
- Muscular pseudohypertrophy and hypothyroidism syndrome716338001
- Oculogastrointestinal muscular dystrophy722060007
- Visceral myopathy with familial external ophthalmoplegia syndrome722060007
- Muscular dystrophy Selcen type723407009
- Selcen muscular dystrophy723407009
- Congenital muscular dystrophy Paradas type725420009
- Congenital myopathy Paradas type725420009
- Distal myopathy Swedish type726107008
- Distal myopathy Welander type726107008
- Distal ABD-filaminopathy733489002
- Distal myopathy with posterior leg and anterior hand involvement733489002
- Congenital muscular dystrophy with hyperlaxity763314009
- Distal myopathy type 3763718009
- Finnish upper limb onset distal myopathy763718009
- KLHL9-related early-onset distal myopathy763776004
- Kelch like family member 9 related early-onset distal myopathy763776004
- OPDM - oculopharyngodistal myopathy763829004
- Oculopharyngeal distal myopathy763829004
- Oculopharyngodistal myopathy763829004
- Distal myopathy type 1764859001
- Gowers disease764859001
- Laing early-onset distal myopathy764859001
- Congenital muscular dystrophy type 1B764944006
- Late-onset distal myopathy Markesbery Griggs type770558006
- ZASP (Z-band alternatively spliced PDZ motif protein) related myofibrillar myopathy770558006
- ZASP related myofibrillar myopathy770558006
- Adult-onset distal myopathy due to VCP (valosin containing protein) mutation770792007
- Adult-onset distal myopathy due to VCP mutation770792007
- Adult-onset distal myopathy due to valosin containing protein mutation770792007
- Congenital muscular dystrophy with ITGA7 (integrin alpha-7) deficiency771267003
- Congenital muscular dystrophy with ITGA7 deficiency771267003
- Congenital muscular dystrophy with integrin alpha-7 deficiency771267003
- Congenital muscular dystrophy due to LMNA (lamin A/C) mutation771272007
- Congenital muscular dystrophy due to LMNA mutation771272007
- Congenital muscular dystrophy due to lamin A/C mutation771272007
- LMNA-related congenital muscular dystrophy771272007
- Distal anterior compartment myopathy782675008
- Distal myopathy with anterior tibial onset782675008
- Carbohydrate deficient glycoprotein syndrome type 1u782772000
- Congenital disorder of glycosylation type 1u782772000
- Congenital muscular dystrophy with intellectual disability and severe epilepsy782772000
- Distal nebulin myopathy783148005
- Nebulin-related early-onset distal myopathy783148005
- Distal anoctaminopathy783166000
- MMD3 - Miyoshi muscular dystrophy type 3783166000
- Miyoshi muscular dystrophy type 3783166000
- Congenital muscular dystrophy with intellectual disability783174004
- Congenital muscular dystrophy without intellectual disability783175003
- Congenital muscular dystrophy with cerebellar involvement783176002
- X-linked scapuloperoneal muscular dystrophy784352007
- X-linked scapuloperoneal syndrome784352007
- Muscle eye brain disease with bilateral multicystic leucodystrophy785298001
- Muscle eye brain disease with bilateral multicystic leukodystrophy785298001
- CMD1A - congenital muscular dystrophy type 1A787037000
- Congenital muscular dystrophy due to laminin alpha2 deficiency787037000
- Congenital muscular dystrophy type 1A787037000
- MCD1A - muscular congenital dystrophy type 1A787037000
- Merosin-negative congenital muscular dystrophy787037000
- Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation890368007
- Congenital muscular dystrophy type 1D large gene mutation890395002
- Autosomal dominant Emery-Dreifuss muscular dystrophy1010712009
- EDMD2 - autosomal dominant Emery-Dreifuss muscular dystrophy1010712009
- Amyotrophy of muscle of shoulder1119438000
- Atrophy of muscle of shoulder1119438000
- Amyotrophy of muscle of lower leg1119440005
- Atrophy of muscle of lower leg1119440005
- Progressive weakness of muscle1137511009
- Pseudohypertrophy of calf muscle1142247001
- Atrophy of peroneal muscle1142324004
- X-linked Emery-Dreifuss muscular dystrophy1156836006
- Autosomal recessive Emery-Dreifuss muscular dystrophy1156848009
- EDMD3 - autosomal recessive Emery-Dreifuss muscular dystrophy1156848009
- Congenital muscular dystrophy Davignon Chauveau type1172688004
- Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome1172688004
- ADSSL1-related distal myopathy1172694007
- Adenylosuccinate synthetase-like 1-related distal myopathy1172694007
- Autosomal recessive limb girdle muscular dystrophy type 2Z1172703004
- Limb girdle muscular dystrophy type 2Z1172703004
- POGLUT1-related limb girdle muscular dystrophy R211172703004
- Protein O-glucosyltransferase 1-related limb girdle muscular dystrophy R211172703004
- Kaeser syndrome1208615009
- Neurogenic scapuloperoneal syndrome Kaeser type1208615009
- Stark Kaeser syndrome1208615009
- Progressive scapulohumeroperoneal distal myopathy1217226000
- Congenital megaconial myopathy1230273004
- Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect1230273004
- Congenital muscular dystrophy with mitochondrial structural abnormalities1230273004
- Megaconial congenital muscular dystrophy1230273004
- Intermediate COL6-RD1348306008
- Intermediate collagen VI-related muscular dystrophy1348306008
- Infantile and/or juvenile cataract342291000119102
UMLS
- Autosomal Dominant Myosin Storage Congenital Myopathy 7AC4759774
- CMYO7AC4759774
- CMYP7AC4759774
- CONGENITAL MYOPATHY 7A, MYOSIN STORAGE, AUTOSOMAL DOMINANTC4759774
- MSMAC4759774
- MYH7-Related Scapuloperoneal MyopathyC4759774
- MYOPATHY WITH LYSIS OF TYPE I MYOFIBRILSC4759774
- MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANTC4759774
- MYOPATHY, MYOSIN STORAGE, AUTOSOMAL DOMINANTC4759774
- Muscular Dystrophy, ScapuloperonealC4759774
- Myopathy, Hyaline Body, Autosomal DominantC4759774
- Myopathy, MYH7-Related ScapuloperonealC4759774
- Myopathy, Myosin StorageC4759774
- Myosin Storage MyopathiesC4759774
- Myosin Storage MyopathyC4759774
- SCAPULOPERONEAL MUSCULAR DYSTROPHYC4759774
- SCAPULOPERONEAL MYOPATHY, MYH7-RELATEDC4759774
- SCAPULOPERONEAL SYNDROME, MYOPATHIC TYPEC4759774
- SPMDC4759774
- SPMMC4759774
- Scapuloperoneal Muscular DystrophyC4759774
- Scapuloperoneal Myopathy, MYH7 RelatedC4759774
- Scapuloperoneal Myopathy, MYH7-RelatedC4759774
- Scapuloperoneal muscular dystrophyC4759774
- Scapuloperoneal muscular dystrophy (disorder)C4759774
- Storage Myopathy, MyosinC4759774
- Benign scapuloperoneal muscular dystrophy with early contractures [Emery-Dreifuss]C2875312
- Congenital muscular dystrophyC0699743
- Congenital muscular dystrophy NOSC0699743
- congenital muscular dystrophyC0699743
- Congenital muscular dystrophy with specific morphological abnormalities of the muscle fiberC3264046
- Distal Muscular DystrophiesC0751336
- Distal Muscular DystrophyC0751336
- Distal MyopathiesC0751336
- Distal MyopathyC0751336
- Distal muscular dystrophyC0751336
- Distal muscular dystrophy (disorder)C0751336
- Distal myopathyC0751336
- Muscular Dystrophies, DistalC0751336
- Muscular Dystrophy, DistalC0751336
- Myopathies, DistalC0751336
- Myopathy, DistalC0751336
- Myopathy, distalC0751336
- distal myopathyC0751336
- Dystrophies, Oculopharyngeal MuscularC0270952
- Dystrophy, Oculopharyngeal MuscularC0270952
- Dystrophy, oculopharyngeal muscularC0270952
- MUSCULAR DYSTROPHY, OCULOPHARYNGEALC0270952
- Muscular Dystrophies, OculopharyngealC0270952
- Muscular Dystrophy, OculopharyngealC0270952
- Muscular dystrophy, oculopharyngealC0270952
- OCULOPHARYNGEAL MUSCULAR DYSTROPHY 1C0270952
- OPMDC0270952
- OPMD1C0270952
- Oculopharyngeal DystrophyC0270952
- Oculopharyngeal Muscular DystrophiesC0270952
- Oculopharyngeal Muscular DystrophyC0270952
- Oculopharyngeal dystrophyC0270952
- Oculopharyngeal muscular dystrophyC0270952
- Oculopharyngeal muscular dystrophy (disorder)C0270952
- Progressive Muscular Dystrophy, Oculopharyngeal TypeC0270952
- Progressive muscular dystrophy, oculopharyngeal typeC0270952
- Ocular muscular dystrophyC0270951
- Other specified muscular dystrophiesC4702817
Frequently Asked Questions
What is the ICD-10 code for other specified muscular dystrophies?
The ICD-10-CM code for other specified muscular dystrophies is G71.09. The full clinical description is "Other specified muscular dystrophies". G71.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code G71.09 mean?
ICD-10-CM code G71.09 represents "Other specified muscular dystrophies". It is classified under Chapter 6: Diseases of the Nervous System and is a billable/specific code that can be used on a claim.
Is G71.09 a billable code?
Yes, G71.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is G71.09 in?
G71.09 is in Chapter 6: Diseases of the Nervous System (codes G00-G99).
What SNOMED CT codes does G71.09 map to?
G71.09 maps to 86 SNOMED CT concepts: 1172694007, 240065009, 770792007, 1119440005, 1119438000, and 81 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for G71.09?
G71.09 is linked to 8 UMLS Concept Unique Identifiers: C4759774, C2875312, C0699743, C3264046, C0751336, and 3 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.