Q79.8
BillableOther congenital malformations of musculoskeletal system
Other congenital malformations of musculoskeletal system
Status
Billable / Specific
Parent Code
Q79Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Absence of muscle
- Absence of tendon
- Accessory muscle
- Amyotrophia congenita
- Congenital constricting bands
- Congenital shortening of tendon
- Poland syndrome
Also Known As / Clinical Terms
SNOMED CT
- Congenital hepatomegaly407000
- Disorder: ectopic bone tissue, congenital26155004
- Ectopic bone tissue, congenital26155004
- Congenital absence of pectoral muscle27262009
- Poland anomalad38371006
- Poland anomaly38371006
- Poland syndrome38371006
- Congenital absence of skeletal muscle38776003
- Congenital absence of abdominal muscle42190000
- Congenital shortening of tendon45987002
- Congenital absence of muscle AND/OR tendon47880003
- Congenital absence of muscle and tendon47880003
- Accessory muscle50847000
- Accessory skeletal muscle50847000
- Bruch-de Lange syndrome55016009
- Congenital muscular hypertrophy-cerebral syndrome55016009
- Accessory ossification center63413008
- Accessory ossification centre63413008
- Congenital hyperplasia of muscle66042003
- Congenital muscular hypertrophy66042003
- Doppellendigkeit66042003
- Myofibrillar hyperplasia66042003
- Abnormal development of cartilage67988000
- Chondrodystrophy67988000
- Congenital anomaly of cartilage67988000
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Amyotrophia congenita75491005
- Carpal synostosis92843003
- Congenital abnormal fusion of carpal bone92843003
- Congenital carpal coalition92843003
- Congenital fused carpal bone92843003
- Congenital anomaly of hyoid bone93005008
- Congenital hypoplasia of hyoid bone93265002
- Congenital small hyoid bone93265002
- Congenital thoracogastroschisis93413002
- Thoracoceloschisis93413002
- Incomplete ossification of hyoid bone93585004
- Reduced ossification of hyoid bone93585004
- Congenital skeletal dysplasia105986008
- Osteochondrodysplasia105986008
- Osteodysplasia105986008
- Skeletal dysplasia105986008
- Congenital absence of skeletal bone127328006
- Congenital short Achilles tendon205093009
- Congenital short quadriceps205111008
- Aberrant forearm flexor muscle205270008
- Hypoplasia of muscle205530002
- Absent muscle205532005
- Aplasia of muscle205532005
- Orbinsky syndrome205532005
- POF - Premature ovarian failure237788002
- Premature ovarian failure237788002
- Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia239010003
- Chondrolysis240139008
- Chondrolysis of articular cartilage240139008
- Aberrant muscle of the upper limb253916007
- GO - Geroderma osteodysplastica254116003
- Geroderma osteodysplastica254116003
- Osteodysplastic geroderma254116003
- Absent tendon271018002
- Congenital absence of tendon271018002
- Congenital anomaly of body cavity363026004
- Constricting band of extremity403556005
- Congenital contracture of gastrocnemius muscle427103005
- Congenital absence of quadriceps muscle432993002
- Congenital absence of part of upper arm449683009
- Muscle hypertrophy syndrome699185005
- Myostatin related hypertrophy of muscle699185005
- KBG syndrome711156009
- Short stature, facial and skeletal anomalies, intellectual disability, macrodontia syndrome711156009
- Short stature-characteristic facies-mental retardation-macrodontia-skeletal anomalies syndrome711156009
- Hadziselimovic syndrome719395001
- Microcephalus facio-cardio-skeletal syndrome Hadziselimovic type719395001
- Microcephaly faciocardioskeletal syndrome719395001
- Dermatoosteolysis Kirghizian type721090002
- Kirghizian dermatoosteolysis721090002
- Foot contracture, muscle atrophy, oculomotor apraxia syndrome722456001
- Intellectual disability, developmental delay, contracture syndrome722456001
- Wieacker Wolff syndrome722456001
- Congenital short costocoracoid ligament725101002
- Congenitally short costocoracoid ligament725101002
- Bone fragility, contractures, arterial rupture, deafness syndrome763318007
- Bone fragillity, contractures, arterial rupture, deafness syndrome763318007
- Connective tissue disorder due to LH3 deficiency763318007
- Connective tissue disorder due to lysyl hydroxylase-3 deficiency763318007
- King Denborough syndrome764957003
- Koussef Nichols syndrome764957003
- Amniotic band syndrome765206003
- Congenital constriction band765206003
- Constriction ring syndrome765206003
- Deformity due to amniotic band765206003
- Angio-osteohypotrophic syndrome765750001
- Angioosteohypotrophic syndrome765750001
- Phlebectatic osteohypoplastic angiodysplasia765750001
- Servelle Martorell syndrome765750001
- Lundberg syndrome770679002
- Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome770679002
- Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome773584001
- Segmental progressive overgrowth syndrome with fibroadipose hyperplasia787094005
- Congenital dysplasia of bone caused by drug897590006
- Drug-induced bone dysplasia897590006
- Congenital hypoplasia of calf muscle1144338005
- Congenital hypoplasia of posterior crural muscle1144338005
- Congenital hypoplasia of biceps brachii muscle1144391002
- Congenital hypoplasia of muscle of upper limb1144392009
- Congenital hypoplasia of deltoid muscle1144568000
- Congenital hypoplasia of latissimus dorsi muscle1144569008
- Congenital hypoplasia of serratus anterior muscle1144570009
- Congenital hypoplasia of muscle of abdominal wall1144571008
- Congenital hypoplasia of muscle of pelvis1144572001
- Congenital hypoplastic muscle of pelvis1144572001
- Congenital hypoplasia of muscle of neck1144573006
- Congenital hypoplasia of muscle of shoulder1144574000
- Congenital hypoplasia of pectoralis minor muscle1144575004
- Congenital hypoplasia of pectoral muscle1144576003
- Congenital hypoplasia of pectoralis major muscle1144577007
- Aplasia of muscle of shoulder1144578002
- Aplasia of muscle of abdominal wall1144579005
- Aplasia of muscle of pelvis1144580008
- Aplasia of pectoral muscle1144581007
- Aplasia of pectoralis major muscle1144582000
- Congenital hypoplasia of muscle of upper arm1145375007
- Congenital hypoplasia of triceps brachii muscle1145376008
- Congenital hypoplasia of muscle of extremity1145377004
- Congenital hypoplasia of muscle of limb1145377004
- Aplasia of muscle of extremity1145378009
- Aplasia of muscle of limb1145378009
- Aplasia of muscle of upper arm1145379001
- Aplasia of muscle of upper limb1145380003
- Aplasia of biceps brachii1145381004
- Congenital hypoplasia of muscle of thigh1145386009
- Aplasia of muscle of thigh1145388005
- Aplasia of quadriceps femoris muscle1145390006
- Congenital hypoplasia of quadriceps femoris muscle1145391005
- Aplasia of triceps brachii1145392003
- Congenital chondrolysis1153394005
- Congenital chondrolysis of articular cartilage1153394005
- Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome1229999001
- Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome1229999001
- Amyoplasia congenita1264194006
- Classic arthrogryposis1264194006
- Congenital amyoplasia1264194006
- Bilateral congenital short achilles tendons15934341000119103
- Congenital bilateral short Achilles tendons15934341000119103
- Congenital shortening of both achilles tendons15934341000119103
- Bilateral muscle contracture of ankle regions15704121000119105
- Contracture of muscle of bilateral ankle regions15704121000119105
- Contracture of muscle of both ankle regions15704121000119105
- Bilateral muscle contracture of lower legs15703761000119104
- Contracture of muscle of bilateral lower legs15703761000119104
- Contracture of muscle of both lower legs15703761000119104
- Muscle contracture of bilateral lower legs15703761000119104
- Congenital absence of bilateral pectoral muscles15669001000119106
- Congenital absence of both pectoral muscles15669001000119106
- Congenital absence of left pectoral muscle15669041000119108
- Congenital absence of right pectoral muscle15669081000119103
- Congenital absence of soft tissue of distal phalanx of finger450441000124103
- Congenital contracture of bilateral gastrocnemius15670361000119106
- Congenital contracture of both gastrocnemius15670361000119106
- Congenital contracture of left gastrocnemius muscle15670321000119101
- Congenital contracture of right gastrocnemius muscle15670281000119106
- Congenital short left Achilles tendon1078201000119106
- Congenital shortening of left Achilles tendon1078201000119106
- Congenital short right Achilles tendon1078191000119108
- Congenital shortening of right Achilles tendon1078191000119108
- Contracture of muscle of left ankle region305281000119104
- Muscle contracture of left ankle305281000119104
- Contracture of muscle of right ankle region305361000119104
- Muscle contracture of right ankle305361000119104
UMLS
- ABSC0220724
- AMNIOTIC BAND SEQUENCEC0220724
- Amniotic Band SequenceC0220724
- Amniotic bands sequenceC0220724
- CONSTRICTING BANDS, CONGENITALC0220724
- Congenital constricting bandsC0220724
- Constricting Bands, CongenitalC0220724
- Familial amniotic bandsC0220724
- STREETER ANOMALYC0220724
- Streeter anomalyC0220724
- Absence of muscleC1456418
- Absence of tendonC0432186
- Absent tendonC0432186
- Congenital absence of tendonC0432186
- Congenital absence of tendon (disorder)C0432186
- Accessory muscleC0158784
- Accessory skeletal muscleC0158784
- Accessory skeletal muscle (disorder)C0158784
- accessory muscleC0158784
- accessory musclesC0158784
- Amyotrophia congenitaC0265520
- Amyotrophia congenita (disorder)C0265520
- Anomaly, PolandC0032357
- POLAND ANOMALYC0032357
- POLAND SEQUENCEC0032357
- POLAND SYNDACTYLYC0032357
- POLAND SYNDROMEC0032357
- Poland AnomalyC0032357
- Poland SequenceC0032357
- Poland SyndactylyC0032357
- Poland SyndromeC0032357
- Poland anomaladC0032357
- Poland anomalyC0032357
- Poland anomaly (disorder)C0032357
- Poland sequenceC0032357
- Poland syndactylyC0032357
- Poland syndromeC0032357
- Poland's anomalyC0032357
- Poland's syndromeC0032357
- Syndactyly, PolandC0032357
- Syndrome PolandsC0032357
- Syndrome, PolandC0032357
- Unilateral defect of pectoralis major and syndactyly of the handC0032357
- anomaly polandsC0032357
- poland anomalyC0032357
- poland syndromeC0032357
- poland's anomalyC0032357
- poland's syndromeC0032357
- polands syndromeC0032357
- Congenital shortening of tendonC0265522
- Congenital shortening of tendon (disorder)C0265522
- Other congenital malformations of musculoskeletal systemC0478080
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.