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ICD-10-CM Codes
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Q00-Q99
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Q65-Q79
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Q79-
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2023 ICD-10-CM Diagnosis Code Q79.8
2023 ICD-10-CM Diagnosis Code Q79.8
Other congenital malformations of musculoskeletal system
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
- Q79.8 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q79.8 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q79.8 - other international versions of ICD-10 Q79.8 may differ.
Applicable To- Absence of muscle
- Absence of tendon
- Accessory muscle
- Amyotrophia congenita
- Congenital constricting bands
- Congenital shortening of tendon
- Poland syndrome
The following code(s) above
Q79.8 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q79.8:
- Absence of pectoral muscle, congenital
- Amniotic band syndrome
- Amyoplasia congenita disruptive sequence
- Amyoplasia, disruptive sequence
- Congenital absence of bilateral pectoral muscles
- Congenital absence of left pectoral muscle
- Congenital absence of pectoral muscle
- Congenital absence of right pectoral muscle
- Congenital anomaly of cartilage
- Congenital cartilage deformity
- Congenital contracture of bilateral gastrocnemius
- Congenital contracture of gastrocnemius muscle
- Congenital contracture of left gastrocnemius
- Congenital contracture of left gastrocnemius muscle
- Congenital contracture of right gastrocnemius
- Congenital contracture of right gastrocnemius muscle
- Congenital deformity of soft tissue
- Contracture of gastrocnemius, congenital
- Deformity due to amniotic band
- Hereditary osteoonychodysplasia
- Nail-patella syndrome
- Nail-patella syndrome, hereditary osteoonychodysplasia
- Poland anomalad
- Poland anomaly
- Popliteal pterygium syndrome
- Schwartz jampel syndrome
- Waardenburg syndrome
- Waardenburg's syndrome
Clinical Information
- A rare developmental disorder characterized by underdevelopment or absence of the pectoralis muscle in one side of the chest, usually associated with ipsilateral cutaneous syndactyly, and ipsilateral breast and nipple hypoplasia.
- A syndrome which is characterized by symbrachydactyly and aplasia of the sternal head of pectoralis major.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q79.8 is considered exempt from POA reporting.
ICD-10-CM Q79.8 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 564 Other musculoskeletal system and connective tissue diagnoses with mcc
- 565 Other musculoskeletal system and connective tissue diagnoses with cc
- 566 Other musculoskeletal system and connective tissue diagnoses without cc/mcc
Convert Q79.8 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
Code annotations containing back-references to Q79.8:
- Absence (of) (organ or part) (complete or partial)
- muscle (congenital) (pectoral) Q79.8
- tendon Q79.8 (congenital)
- Accessory (congenital)
- bone NEC Q79.8
- muscle Q79.8
- tendon Q79.8
- Acromicria, acromikria Q79.8
- Agenesis
- muscle Q79.8
- musculoskeletal system NEC Q79.8
- tendon Q79.8
- Amyoplasia congenita Q79.8
- Amyotrophia, amyotrophy, amyotrophic G71.8
ICD-10-CM Diagnosis Code G71.8
Other primary disorders of muscles
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- Band(s)
- constricting, congenital Q79.8
- Contraction(s)
- ligament - see also Disorder, ligament
- muscle (postinfective) (postural) M62.40
ICD-10-CM Diagnosis Code M62.40
Contracture of muscle, unspecified site
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- Diastasis
- muscle M62.00
ICD-10-CM Diagnosis Code M62.00
Separation of muscle (nontraumatic), unspecified site
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- Dysplasia - see also Anomaly
- Fusion, fused (congenital)
- Hypoplasia, hypoplastic
- Krabbe's
- syndrome, congenital muscle hypoplasia Q79.8
- Myelo-osteo-musculodysplasia hereditaria Q79.8
- Poland syndrome Q79.8
- Short, shortening, shortness
- Supernumerary (congenital)
- Syndrome - see also Disease
- Krabbe's congenital muscle hypoplasia Q79.8
- Touraine's Q79.8
- Thoracogastroschisis Q79.8 (congenital)
- Touraine's syndrome Q79.8
ICD-10-CM Codes Adjacent To Q79.8
Q79.4 Prune belly syndrome
Q79.5 Other congenital malformations of abdominal wall
Q79.51 Congenital hernia of bladder
Q79.59 Other congenital malformations of abdominal wall
Q79.6 Ehlers-Danlos syndromes
Q79.60 Ehlers-Danlos syndrome, unspecified
Q79.61 Classical Ehlers-Danlos syndrome
Q79.62 Hypermobile Ehlers-Danlos syndrome
Q79.63 Vascular Ehlers-Danlos syndrome
Q79.69 Other Ehlers-Danlos syndromes
Q79.8
Other congenital malformations of musculoskeletal system
Q79.9 Congenital malformation of musculoskeletal system, unspecified
Q80 Congenital ichthyosis
Q80.0 Ichthyosis vulgaris
Q80.1 X-linked ichthyosis
Q80.2 Lamellar ichthyosis
Q80.3 Congenital bullous ichthyosiform erythroderma
Q80.8 Other congenital ichthyosis
Q80.9 Congenital ichthyosis, unspecified
Q81 Epidermolysis bullosa
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
