Diagnosis Code

Q78.8 OTHER SPECIFIED OSTEOCHONDRODYSPLASIAS


Code Information

Diagnosis Code: Q78.8

Short Description: Other specified osteochondrodysplasias

Long Description: Other specified osteochondrodysplasias

The code Q78.8 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
      • Other osteochondrodysplasias (Q78)
        • Q78.8 Other specified osteochondrodysplasias

Code Version: 2022 ICD-10-CM


Synonyms

  • Acrocapitofemoral dysplasia
  • Acrodysostosis
  • Acromesomelic dysplasia Hunter-Thompson type
  • Acromesomelic dysplasia Maroteaux type
  • Acroosteolysis
  • Acroosteolysis
  • Acroosteolysis
  • Acropectorovertebral dysplasia
  • Agenesis of fibula
  • Aluminum bone disease
  • Aluminum-related fracturing osteodystrophy
  • Angel-shaped phalangoepiphyseal dysplasia
  • Atelosteogenesis
  • Atelosteogenesis type 1
  • Atelosteogenesis type 2
  • Atelosteogenesis type 3
  • Autosomal dominant omodysplasia
  • Autosomal dominant retinitis pigmentosa
  • Autosomal recessive omodysplasia
  • Beals auriculo-osteodysplasia syndrome
  • Bent bone dysplasia group
  • Blomstrand dysplasia
  • Bone dysplasia lethal Holmgren type
  • Boomerang dysplasia
  • Bowing of upper limb
  • Bruck syndrome
  • Carpal-tarsal osteolysis with nephropathy
  • Carpotarsal osteochondromatosis
  • Cerebral degeneration in childhood
  • Chitty Hall Baraitser syndrome
  • Chronic deafness
  • CHST3-related skeletal dysplasia
  • Cleidorhizomelic syndrome
  • Cole-Carpenter dysplasia
  • Colobomatous microphthalmia, rhizomelic dysplasia syndrome
  • Complex lethal osteochondrodysplasia
  • Congenital abnormal fusion of humerus
  • Congenital abnormal shape of humerus
  • Congenital abnormal shape of radius
  • Congenital absence of pectoral muscle
  • Congenital anomalies of elbow and upper arm
  • Congenital deformity of bone of forearm
  • Congenital exostosis
  • Congenital hypoplasia of fibula
  • Congenital hypoplasia of tibia
  • Congenital hypoplasia of ulna
  • Congenital nephritis
  • Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome
  • Craniofrontonasal dysplasia with Poland anomaly syndrome
  • Craniometadiaphyseal dysplasia
  • Craniometadiaphyseal dysplasia wormian bone type
  • Craniometaphyseal dysplasia
  • Dacryocystitis and osteopoikilosis syndrome
  • Dappled diaphyseal dysplasia
  • Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome
  • Deformity of radius
  • Dermatofibrosis lenticularis disseminata
  • Desbuquois syndrome
  • Diaphanospondylodysostosis
  • Disorganized development of cartilaginous and fibrous components of the skeleton
  • Disuse osteodystrophy
  • Dyschondrosteosis and nephritis syndrome
  • Dysosteosclerosis
  • Dysostosis
  • Dysplasia with defective mineralization
  • Dysplasia with increased bone density
  • Dysplasias with significant membranous bone involvement
  • Dysplastic cortical hyperostosis
  • Early-onset calcifying leukoencephalopathy, skeletal dysplasia
  • Enchondromatosis
  • Endocrine-cerebro-osteodysplasia syndrome
  • Endosteal hyperostoses
  • Endosteal hyperostoses
  • Endosteal hyperostoses with cerebellar hypoplasia
  • Epilepsy, microcephaly, skeletal dysplasia syndrome
  • Epiphyseal dysplasia
  • Epiphyseal dysplasia, hearing loss, dysmorphism syndrome
  • Epiphyseal dysplasia, microcephalus, nystagmus syndrome
  • Familial osteodysplasia Anderson type
  • FGFR2-related bent bone dysplasia
  • Fibrochondrogenesis
  • Frontometaphyseal dysplasia
  • Frontonasal dysplasia sequence
  • Geleophysic dysplasia
  • Genochondromatosis
  • Genochondromatosis type 1
  • Genochondromatosis type 2
  • Giacci familial neurogenic acroosteolysis
  • Gnathodiaphyseal dysplasia
  • Grant syndrome
  • Hair discoloration
  • Hajdu-Cheney syndrome
  • Heide syndrome
  • Hepatic osteodystrophy
  • Hereditary acroosteolysis
  • Humeroulnar synostosis
  • Hyperphosphatasemia tarda
  • Idiopathic hypoparathyroidism
  • Idiopathic osteolyses
  • Idiopathic osteolyses
  • Immuno-osseous dysplasia
  • Immuno-osseous dysplasia
  • Immuno-osseous dysplasia
  • Immuno-osseous dysplasia
  • Infantile cortical hyperostosis
  • Isolated osteopoikilosis
  • Kenny syndrome
  • Kniest dysplasia
  • Kniest-Stickler dysplasia
  • Kyphomelic dysplasia
  • Larsen-like osseous dysplasia, short stature syndrome
  • Larsen-like syndrome B3GAT3 type
  • Lenz-Majewski hyperostosis syndrome
  • Leri's pleonosteosis syndrome
  • Lethal chondrodysplasia with fragmented bone
  • Lethal Kniest-like syndrome
  • Lethal occipital encephalocele, skeletal dysplasia syndrome
  • Lethal recessive chondrodysplasia
  • Leukoencephalopathy with metaphyseal chondrodysplasia syndrome
  • Longitudinal deficiency of foot
  • LRP5-related primary osteoporosis
  • Madelung's deformity
  • Melhem Fahl syndrome
  • Melnick-Needles syndrome
  • Melorheostosis
  • Melorheostosis with osteopoikilosis
  • Mesomelic dysplasia
  • Mesomelic dysplasia Kantaputra type
  • Mesomelic dysplasia of upper limb
  • Mesomelic dysplasia Savarirayan type
  • Metachondromatosis
  • Metaphyseal anadysplasia
  • Metaphyseal chondrodysplasia Kaitila type
  • Metatropic dysplasia
  • Microcephalic osteodysplastic dysplasia Saul Wilson type
  • Microcephalic osteodysplastic primordial dwarfism type II
  • Microcephalic osteodysplastic primordial dwarfism types I and III
  • Mixed sclerosing bone dysplasia
  • Mixed sclerosing bone dystrophy with extra-skeletal manifestation
  • Multiple dislocations with dysplasia
  • Multiple epiphyseal dysplasia
  • Multiple epiphyseal dysplasia due to collagen 9 anomaly
  • Multiple epiphyseal dysplasia Lowry type
  • Multiple epiphyseal dysplasia tarda type IIIa
  • Multiple epiphyseal dysplasia type 1
  • Multiple epiphyseal dysplasia type 4
  • Multiple epiphyseal dysplasia type 5
  • Multiple epiphyseal dysplasia with miniepiphyses
  • Multiple epiphyseal dysplasia with severe proximal femoral dysplasia
  • Multiple synostosis syndrome
  • NEK9-related lethal skeletal dysplasia
  • Neonatal osteosclerotic dysplasia
  • Occipital encephalocele
  • Omodysplasia
  • Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome
  • Osteochondroma of bone
  • Osteocraniostenosis
  • Osteodysplastic dysplasia, type I
  • Osteodysplastic dysplasia, type II
  • Osteodysplastic primordial dwarfism
  • Osteodysplastic primordial dwarfism
  • Osteodysplastic primordial dwarfism
  • Osteodysplastic primordial dwarfism
  • Osteofibrous dysplasia
  • Osteoglophonic dysplasia
  • Osteopathia striata
  • Osteopathia striata
  • Osteopathia striata, pigmentary dermopathy, white forelock syndrome
  • Osteoplastic dysplasia
  • Osteoplastic dysplasia
  • Osteopoikilosis
  • Osteopoikilosis
  • Osteopoikilosis
  • Otopalatodigital syndrome spectrum disorder
  • Otopalatodigital syndrome spectrum disorder
  • Otopalatodigital syndrome spectrum disorder
  • Pachydermoperiostosis - familial
  • Pacman dysplasia
  • Peripheral dysostosis
  • Poland anomaly
  • Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
  • Precocious osteodysplasty
  • Progressive pseudorheumatoid dysplasia
  • Pseudodiastrophic dysplasia
  • Pyknoachondrogenesis
  • Pyknodysostosis
  • QRICH1-related intellectual disability, chondrodysplasia syndrome
  • Raine dysplasia
  • Reardon Hall Slaney syndrome
  • Reinhardt Pfeiffer mesomelic dysplasia
  • Rhizomelic dysplasia Patterson Lowry type
  • Rhizomelic syndrome Urbach type
  • RHYNS syndrome
  • Rolland-Debuqois syndrome
  • Schimke immuno-osseous dysplasia
  • Sclerosteosis
  • SHOX-related short stature
  • Skeletal dysplasia with epilepsy and short stature syndrome
  • Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome
  • Smith McCort dysplasia
  • Spondylocarpotarsal synostosis syndrome
  • Spondylodysplasia, Luton type
  • Spondylodysplasia, San Diego type
  • Spondylodysplasia, Torrance type
  • Spondylodysplastic group
  • Spondyloenchondrodysplasia
  • Spondyloenchondrodysplasia with immune dysregulation
  • Spondyloepimetaphyseal dysplasia, Strudwick type
  • Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Spondylometaphyseal dysplasia Schmidt type
  • Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome
  • Spondylo-ocular syndrome
  • Stenosis of lacrimal canaliculi
  • Stuve-Wiedemann dysplasia
  • Syndromic nanophthalmos due to Kenny-Caffey syndrome
  • Terminal osseous dysplasia and pigmentary defect syndrome
  • Variation in hair color
  • Velofacioskeletal syndrome
  • Weismann Netter syndrome
  • White forelock
  • Whyte Hemingway carpal tarsal phalangeal osteolyses
  • X-linked calvarial hyperostosis
  • X-linked dominant chondrodysplasia Chassaing Lacombe type
  • X-linked osteoporosis with fractures
  • Yunis-Varon dysplasia

Diagnostic Related Group(s)

The code Q78.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
  • Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

References to Index of Diseases and Injuries

The code Q78.8 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Osteopoikilosis

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q78.8 Right Arrow 756.53 Osteopoikilosis
756.59 Osteodystrophy NEC

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q78 Other osteochondrodysplasias
Q78.0 Osteogenesis imperfecta
Q78.1 Polyostotic fibrous dysplasia
Q78.2 Osteopetrosis
Q78.3 Progressive diaphyseal dysplasia
Q78.4 Enchondromatosis
Q78.5 Metaphyseal dysplasia
Q78.6 Multiple congenital exostoses
Q78.9 Osteochondrodysplasia, unspecified


This page was last updated on: 10/1/2023