Congenital abnormal slender shape of diaphysis of long bone
Congenital musculoskeletal anomaly
Cone shaped epiphysis with epiphyseal arrest
CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome
Congenital abnormal triangular shape of epiphysis
MUSCULOSKELETAL ABNORM
Abnormalities, Musculoskeletal
ABNORM MUSCULOSKELETAL
Aberrant muscle of the lower limb
Congenital skeletal anomaly
Au Kline syndrome
Ambiguous genitalia
Congenital deformity of musculoskeletal system NOS
Multiple bony abnormalities
Angioosteohypertrophic syndrome
46,XX disorder of sex development with skeletal anomalies syndrome
Marfanoid physique
CODAS syndrome
Congenital abnormality of musculoskeletal system
Congenital anomaly of skeletal bone
Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome
Congenital deformity of musculoskeletal system
Congenital lordosis deformity of spine
Okamoto syndrome
Slender long bone
Congenital Musculoskeletal Defect
Congenital musculoskeletal abnormality NOS
Congenital abnormal cone shape of epiphysis with epiphyseal arrest
Congenital malformation of muscles and tendons
Combined malformation of central nervous system and skeletal muscle
Abnormality, Musculoskeletal
Congenital musculoskeletal abnormality
Congenital abnormal slender shape of long bone
Nathalie syndrome
Congenital anomaly of musculoskeletal system (disorder)
Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome
Congenital anomaly of musculoskeletal system NOS
SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome
Musculoskeletal Abnormalities
Musculoskeletal Abnormality
Musculoskeletal congenital anomaly
Angio-osteohypertrophic syndrome
Deafness with cataract and skeletal anomaly syndrome
Van Maldergem syndrome
Triangular shaped epiphysis
Aplasia of bone of axial skeleton
Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
Cerebro-oculo-dento-auriculo-skeletal syndrome
SCARF syndrome
Congenital anomaly of abdomen
Slender shape of diaphysis of long bone
Congenital anomaly of musculoskeletal system
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
Short long bone
Congenital deformity of musculoskeletal system (disorder)
Female pseudohermaphroditism with skeletal anomalies syndrome
Congenital anomaly of bone and joint
Abnormally short long bone
Congenital malformation of skeletal bone
Anomaly of skeletal development
Muscle eye brain disease
ZTTK syndrome
Anomaly congenital musculoskeletal (NOS)
Bone absent
Cerebrofacioarticular syndrome
Congenital anomaly of muscle AND/OR tendon
Congenital lordosis deformity of spine due to congenital malformation of skeletal bone
Zhu Tokita Takenouchi Kim syndrome
Cyprus facial neuromusculoskeletal syndrome
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
Congenital anomaly of musculoskeletal structure of trunk

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.

How does Q79.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of musculoskeletal system, unsp 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 Q79.9?

Q79.9 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.