Osteodysplasia
POLAND SYNDROME
Aplasia of biceps brachii
Congenital contracture of left gastrocnemius muscle
Congenital abnormal fusion of carpal bone
Bilateral congenital short achilles tendons
Congenital contracture of both gastrocnemius
Carpal synostosis
Absence of tendon
Poland syndactyly
Congenital hypoplasia of biceps brachii muscle
Aplasia of pectoral muscle
Hadziselimovic syndrome
Congenital shortening of right Achilles tendon
Micromelus
Congenital bilateral short Achilles tendons
Congenital short quadriceps
Premature ovarian failure
Congenital hypoplasia of muscle of limb
Congenital dysplasia of bone caused by drug
Congenital hypoplasia of muscle of upper arm
Muscle contracture of right ankle
Thoracoceloschisis
Congenital absence of muscle AND/OR tendon
Micromelic dwarf
Congenital hypoplasia of muscle of abdominal wall
Congenital hypoplasia of quadriceps femoris muscle
Congenital hypoplasia of muscle of extremity
Congenital hypoplasia of triceps brachii muscle
Contracture of muscle of left ankle region
Aplasia of muscle of extremity
Congenital absence of abdominal muscle
Congenital hypoplastic muscle of pelvis
GO - Geroderma osteodysplastica
Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type
Congenital constricting bands
Congenital hypoplasia of muscle of thigh
Chondrodystrophy
Bone fragility, contractures, arterial rupture, deafness syndrome
Congenital contracture of gastrocnemius muscle
Congenital anomaly of hyoid bone
King Denborough syndrome
Poland anomalad
Kirghizian dermatoosteolysis
Poland anomaly
Muscle contracture of bilateral lower legs
Servelle Martorell syndrome
Contracture of muscle of both ankle regions
STREETER ANOMALY
Constricting Bands, Congenital
Poland anomaly (disorder)
Angio-osteohypotrophic syndrome
Congenital fused carpal bone
Classic arthrogryposis
Unilateral defect of pectoralis major and syndactyly of the hand
Poland Sequence
Congenital muscular hypertrophy-cerebral syndrome
Congenital absence of left pectoral muscle
Syndactyly, Poland
Congenital contracture of right gastrocnemius muscle
Familial amniotic bands
Bilateral muscle contracture of ankle regions
Congenital constriction band
Congenital absence of both pectoral muscles
Doppellendigkeit
Congenital absence of pectoral muscle
Congenital short right Achilles tendon
Constriction ring syndrome
Congenital hypoplasia of serratus anterior muscle
Connective tissue disorder due to LH3 deficiency
Constricting band of extremity
Aplasia of quadriceps femoris muscle
Congenital shortening of tendon (disorder)
Osteochondrodysplasia
Wieacker Wolff syndrome
Accessory skeletal muscle
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
Congenital shortening of tendon
Poland's anomaly
Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome
Congenital absence of part of upper arm
Aplasia of muscle of thigh
Congenital contracture of bilateral gastrocnemius
Contracture of muscle of both lower legs
Congenital anomaly of cartilage
Congenital short left Achilles tendon
Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome
Congenital hypoplasia of deltoid muscle
Congenital skeletal dysplasia
Contracture of muscle of bilateral lower legs
Congenitally short costocoracoid ligament
Accessory ossification center
Aplasia of muscle of upper arm
Accessory muscle
Congenital anomaly of body cavity
Microcephaly faciocardioskeletal syndrome
Amniotic bands sequence
Congenital absence of skeletal bone
Incomplete ossification of hyoid bone
Amyotrophia congenita (disorder)
polands syndrome
Absent tendon
Congenital absence of soft tissue of distal phalanx of finger
Congenital hypoplasia of muscle of pelvis
Abnormal development of cartilage
POF - Premature ovarian failure
Congenital absence of muscle and tendon
Absent muscle
Congenital absence of tendon (disorder)
Amniotic band syndrome
Bruch-de Lange syndrome
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia
Aplasia of muscle
Congenital hypoplasia of muscle of shoulder
Congenital hypoplasia of pectoral muscle
Aplasia of muscle of abdominal wall
Myostatin related hypertrophy of muscle
Ectopic bone tissue, congenital
Congenital hypoplasia of posterior crural muscle
Congenital hypoplasia of hyoid bone
Anomaly, Poland
Congenital absence of bilateral pectoral muscles
Aberrant forearm flexor muscle
Accessory ossification centre
Congenital carpal coalition
Hypoplasia of muscle
Amniotic Band Sequence
Aberrant muscle of the upper limb
Congenital shortening of left Achilles tendon
Amyotrophia congenita
Congenital absence of right pectoral muscle
Accessory skeletal muscle (disorder)
Bone fragillity, contractures, arterial rupture, deafness syndrome
Dermatoosteolysis Kirghizian type
Congenital small hyoid bone
Phlebectatic osteohypoplastic angiodysplasia
poland's syndrome
Bilateral muscle contracture of lower legs
Congenital thoracogastroschisis
Drug-induced bone dysplasia
Amyoplasia congenita
Congenital shortening of both achilles tendons
Contracture of muscle of bilateral ankle regions
Geroderma osteodysplastica
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
Myofibrillar hyperplasia
Aplasia of triceps brachii
Congenital chondrolysis of articular cartilage
KBG syndrome
Chondrolysis
Congenital absence of tendon
Chondrolysis of articular cartilage
Koussef Nichols syndrome
Contracture of muscle of right ankle region
Intellectual disability, developmental delay, contracture syndrome
Congenital absence of quadriceps muscle
Congenital absence of skeletal muscle
Foot contracture, muscle atrophy, oculomotor apraxia syndrome
Congenital short Achilles tendon
Deformity due to amniotic band
Micromelia
Congenital hepatomegaly
Aplasia of pectoralis major muscle
Syndrome Polands
Congenital hyperplasia of muscle
Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome
Muscle contracture of left ankle
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Aplasia of muscle of shoulder
Skeletal dysplasia
Congenital hypoplasia of muscle of upper limb
Congenital hypoplasia of muscle of neck
Congenital hypoplasia of pectoralis minor muscle
Congenital hypoplasia of latissimus dorsi muscle
Reduced ossification of hyoid bone
Congenital amyoplasia
Congenital muscular hypertrophy
Lundberg syndrome
Syndrome, Poland
Muscle hypertrophy syndrome
Aplasia of muscle of pelvis
Osteodysplastic geroderma
Absence of muscle
Congenital short costocoracoid ligament
Disorder: ectopic bone tissue, congenital
Congenital hypoplasia of pectoralis major muscle
Aplasia of muscle of limb
Congenital hypoplasia of calf muscle
accessory muscles
Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome
Nanomelia
anomaly polands
Orbinsky syndrome
ABS
Congenital chondrolysis
Angioosteohypotrophic syndrome
Aplasia of muscle of upper limb

Frequently Asked Questions

What is the ICD-10 code for other congenital malformations of musculoskeletal system?

The ICD-10-CM code for other congenital malformations of musculoskeletal system is Q79.8. The full clinical description is "Other congenital malformations of musculoskeletal system". Q79.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q79.8 mean?

ICD-10-CM code Q79.8 represents “Other congenital malformations of musculoskeletal system”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q79.8 a billable code?

Yes, Q79.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q79.8 in?

Q79.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q79.8 map to?

Q79.8 maps to 99 SNOMED CT concepts: 205270008, 253916007, 67988000, 205532005, 271018002, and 94 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q79.8?

Q79.8 is linked to 8 UMLS Concept Unique Identifiers: C0220724, C1456418, C0432186, C0158784, C0265520, and 3 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q79.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of musculoskeletal system affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q79.8?

Q79.8 maps to the ICD-11 code: LD0Z (Structural developmental anomalies primarily affecting one body system, unspecified).

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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.