ICD-10 block
Q65–Q79 Congenital malformations and deformations of the musculoskeletal system
The block Q65–Q79 of ICD-10 is titled “Congenital malformations and deformations of the musculoskeletal system”. It is part of Chapter XVII, Congenital malformations, deformations and chromosomal abnormalities, and holds 15 groups.
Codes in Q65–Q79
- Q65.0Congenital dislocation of hip, unilateral
- Q65.1Congenital dislocation of hip, bilateral
- Q65.2Congenital dislocation of hip, unspecified
- Q65.3Congenital subluxation of hip, unilateral
- Q65.4Congenital subluxation of hip, bilateral
- Q65.5Congenital subluxation of hip, unspecified
- Q65.6Unstable hip
- Q65.8Other congenital deformities of hip
- Q65.9Congenital deformity of hip, unspecified
- Q66.0Talipes equinovarus
- Q66.1Talipes calcaneovarus
- Q66.2Metatarsus varus
- Q66.3Other congenital varus deformities of feet
- Q66.4Talipes calcaneovalgus
- Q66.5Congenital pes planus
- Q66.6Other congenital valgus deformities of feet
- Q66.7Pes cavus
- Q66.8Other congenital deformities of feet
- Q66.9Congenital deformity of feet, unspecified
- Q68.0Congenital deformity of sternocleidomastoid muscle
- Q68.1Congenital deformity of hand
- Q68.2Congenital deformity of knee
- Q68.3Congenital bowing of femur
- Q68.4Congenital bowing of tibia and fibula
- Q68.5Congenital bowing of long bones of leg, unspecified
- Q68.8Other specified congenital musculoskeletal deformities
- Q71.0Congenital complete absence of upper limb(s)
- Q71.1Congenital absence of upper arm and forearm with hand present
- Q71.2Congenital absence of both forearm and hand
- Q71.3Congenital absence of hand and finger(s)
- Q71.4Longitudinal reduction defect of radius
- Q71.5Longitudinal reduction defect of ulna
- Q71.6Lobster-claw hand
- Q71.8Other reduction defects of upper limb(s)
- Q71.9Reduction defect of upper limb, unspecified
- Q72.0Congenital complete absence of lower limb(s)
- Q72.1Congenital absence of thigh and lower leg with foot present
- Q72.2Congenital absence of both lower leg and foot
- Q72.3Congenital absence of foot and toe(s)
- Q72.4Longitudinal reduction defect of femur
- Q72.5Longitudinal reduction defect of tibia
- Q72.6Longitudinal reduction defect of fibula
- Q72.7Split foot
- Q72.8Other reduction defects of lower limb(s)
- Q72.9Reduction defect of lower limb, unspecified
- Q74.0Other congenital malformations of upper limb(s), including shoulder girdle
- Q74.1Congenital malformation of knee
- Q74.2Other congenital malformations of lower limb(s), including pelvic girdle
- Q74.3Arthrogryposis multiplex congenita
- Q74.8Other specified congenital malformations of limb(s)
- Q74.9Unspecified congenital malformation of limb(s)
- Q76.0Spina bifida occulta
- Q76.1Klippel-Feil syndrome
- Q76.2Congenital spondylolisthesis
- Q76.3Congenital scoliosis due to congenital bony malformation
- Q76.4Other congenital malformations of spine, not associated with scoliosis
- Q76.5Cervical rib
- Q76.6Other congenital malformations of ribs
- Q76.7Congenital malformation of sternum
- Q76.8Other congenital malformations of bony thorax
- Q76.9Congenital malformation of bony thorax, unspecified
- Q77.0Achondrogenesis
- Q77.1Thanatophoric short stature
- Q77.2Short rib syndrome
- Q77.3Chondrodysplasia punctata
- Q77.4Achondroplasia
- Q77.5Dystrophic dysplasia
- Q77.6Chondroectodermal dysplasia
- Q77.7Spondyloepiphyseal dysplasia
- Q77.8Other osteochondrodysplasia with defects of growth of tubular bones and spine
- Q77.9Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
- Q79.0Congenital diaphragmatic hernia
- Q79.1Other congenital malformations of diaphragm
- Q79.2Exomphalos
- Q79.3Gastroschisis
- Q79.4Prune belly syndrome
- Q79.5Other congenital malformations of abdominal wall
- Q79.6Ehlers-Danlos syndrome
- Q79.8Other congenital malformations of musculoskeletal system
- Q79.9Congenital malformation of musculoskeletal system, unspecified
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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