Q79.9
BillableCongenital malformation of musculoskeletal system, unsp
Congenital malformation of musculoskeletal system, unspecified
Status
Billable / Specific
Parent Code
Q79Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly of musculoskeletal system NOS
- Congenital deformity of musculoskeletal system NOS
Also Known As / Clinical Terms
SNOMED CT
- Anomaly of skeletal development8447006
- Congenital anomaly of skeletal bone8447006
- Congenital malformation of skeletal bone8447006
- Congenital skeletal anomaly8447006
- Ambiguous genitalia21321009
- Congenital abnormality of musculoskeletal system73573004
- Congenital anomaly of musculoskeletal system73573004
- Congenital malformation of musculoskeletal system73573004
- Congenital musculoskeletal abnormality73573004
- Congenital anomaly of muscle AND/OR tendon79191007
- Congenital malformation of muscles and tendons79191007
- Aberrant muscle of the lower limb205365003
- Congenital anomaly of bone and joint237513002
- Marfanoid physique248298009
- Multiple bony abnormalities271774001
- Combined malformation of central nervous system and skeletal muscle277949001
- Muscle eye brain disease277950001
- Bone absent298350001
- Congenital anomaly of abdomen363024001
- Congenital anomaly of musculoskeletal structure of trunk363032009
- Deafness with cataract and skeletal anomaly syndrome716170005
- Nathalie syndrome716170005
- CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome717772000
- CODAS syndrome717772000
- Cerebro-oculo-dento-auriculo-skeletal syndrome717772000
- Angio-osteohypertrophic syndrome723991007
- Angioosteohypertrophic syndrome723991007
- Cyprus facial neuromusculoskeletal syndrome732261005
- 46,XX disorder of sex development with skeletal anomalies syndrome733621007
- Female pseudohermaphroditism with skeletal anomalies syndrome733621007
- SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome734173003
- SCARF syndrome734173003
- Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome734173003
- Cerebrofacioarticular syndrome763353000
- Van Maldergem syndrome763353000
- Congenital abnormal slender shape of long bone896706003
- Slender long bone896706003
- Congenital abnormal slender shape of diaphysis of long bone896729006
- Slender shape of diaphysis of long bone896729006
- Congenital abnormal triangular shape of epiphysis896834003
- Triangular shaped epiphysis896834003
- Abnormally short long bone897495004
- Short long bone897495004
- Cone shaped epiphysis with epiphyseal arrest897635007
- Congenital abnormal cone shape of epiphysis with epiphyseal arrest897635007
- Aplasia of bone of axial skeleton1144859006
- Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome1169355000
- ZTTK syndrome1169355000
- Zhu Tokita Takenouchi Kim syndrome1169355000
- Congenital lordosis deformity of spine due to congenital malformation of skeletal bone1187292000
- Congenital lordosis deformity of spine1187358001
- Au Kline syndrome1222710008
- Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome1222710008
- Okamoto syndrome1222710008
- Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome1303865002
- Congenital deformity of musculoskeletal system1344689004
UMLS
- ABNORM MUSCULOSKELETALC0151491
- Abnormalities, MusculoskeletalC0151491
- Abnormality, MusculoskeletalC0151491
- Anomaly congenital musculoskeletal (NOS)C0151491
- Congenital Musculoskeletal DefectC0151491
- Congenital abnormality of musculoskeletal systemC0151491
- Congenital anomaly of musculoskeletal systemC0151491
- Congenital anomaly of musculoskeletal system (disorder)C0151491
- Congenital anomaly of musculoskeletal system NOSC0151491
- Congenital deformity of musculoskeletal systemC0151491
- Congenital deformity of musculoskeletal system (disorder)C0151491
- Congenital deformity of musculoskeletal system NOSC0151491
- Congenital malformation of musculoskeletal systemC0151491
- Congenital malformation of musculoskeletal system, unspC0151491
- Congenital malformation of musculoskeletal system, unspecifiedC0151491
- Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)C0151491
- Congenital musculoskeletal abnormalityC0151491
- Congenital musculoskeletal abnormality NOSC0151491
- Congenital musculoskeletal anomalyC0151491
- MUSCULOSKELETAL ABNORMC0151491
- Musculoskeletal AbnormalitiesC0151491
- Musculoskeletal AbnormalityC0151491
- Musculoskeletal congenital anomalyC0151491
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of musculoskeletal system, unsp?
The ICD-10-CM code for congenital malformation of musculoskeletal system, unsp is Q79.9. The full clinical description is "Congenital malformation of musculoskeletal system, unspecified". Q79.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q79.9 mean?
ICD-10-CM code Q79.9 represents "Congenital malformation of musculoskeletal system, unspecified". 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 Q79.9 a billable code?
Yes, Q79.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q79.9 in?
Q79.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q79.9 map to?
Q79.9 maps to 32 SNOMED CT concepts: 733621007, 205365003, 897495004, 21321009, 723991007, and 27 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q79.9?
Q79.9 is linked to 1 UMLS Concept Unique Identifier: C0151491. 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.