Q78.8
BillableOther specified osteochondrodysplasias
Other specified osteochondrodysplasias
Status
Billable / Specific
Parent Code
Q78Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Lenz-Majewski dysplasia1393001
- Lenz-Majewski hyperostosis syndrome1393001
- Cerebral degeneration in childhood2584003
- Buschke-Ollendorff syndrome9147009
- Osteopoikilosis9147009
- Variation in hair color12168009
- Variation in hair colour12168009
- Melnick-Needles syndrome13449007
- Osteodysplasty13449007
- Fibrochondrogenesis17144009
- Sclerosteosis17568006
- Metatropic dwarf22764001
- Metatropic dwarfism22764001
- Metatropic dwarfism syndrome22764001
- Metatropic dysplasia22764001
- Metatropic dysplasia group22764001
- Caffey disease24752008
- Caffey syndrome24752008
- Caffey's disease24752008
- Familial infantile cortical hyperostosis24752008
- Infantile cortical hyperostosis24752008
- Acroosteolysis27201004
- Congenital absence of pectoral muscle27262009
- Hepatic osteodystrophy28193003
- Geleophysic dwarfism syndrome28557005
- Geleophysic dysplasia28557005
- Craniometaphyseal dysplasia36601008
- Poland anomalad38371006
- Poland anomaly38371006
- Poland syndrome38371006
- Leri pleonosteosis syndrome41656005
- Leri's pleonosteosis syndrome41656005
- Occipital encephalocele42376006
- Atelosteogenesis43814000
- Beals auriculo-osteodysplasia syndrome50123005
- Kniest chondrodystrophy53974002
- Kniest dysplasia53974002
- Kniest syndrome53974002
- Swiss cheese cartilage dysplasia53974002
- Hair discoloration59571007
- Hair discolouration59571007
- Fairbanks-Ribbing type epiphyseal dysplasia59708000
- MED - Multiple epiphyseal dysplasia59708000
- Multiple epiphyseal dysplasia59708000
- Hyperostosis corticalis generalisata59763006
- Hyperphosphatasaemia tarda59763006
- Hyperphosphatasemia tarda59763006
- Hyperphosphatasia tarda59763006
- Leontiasis ossea generalisata59763006
- Van Buchem disease59763006
- van Buchem's syndrome59763006
- Buschke-Ollendorf syndrome60399005
- Dermato-osteopoikilosis60399005
- Dermatofibrosis lenticularis disseminata60399005
- Disseminated dermatofibrosis60399005
- Disuse osteodystrophy60914006
- Multiple synostosis syndrome62628008
- Symphalangism syndrome62628008
- FMD - Frontometaphyseal dysplasia62803002
- Frontometaphyseal dysplasia62803002
- Acroosteolysis syndrome63122002
- Arthro-dento-osteo dysplasia63122002
- Cheney syndrome63122002
- Familial acroosteolysis syndrome63122002
- Hajdu-Cheney syndrome63122002
- Acrodysostosis66758006
- Stenosis of lacrimal canaliculi81345003
- Stenosis of lacrimal canaliculus81345003
- Stenosis of lacrimal passage81345003
- Osteopathia striata82663009
- Voorhoeve's disease82663009
- Kenny syndrome82837002
- Kenny-Caffey syndrome82837002
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- Maroteaux-Lamy pyknodysostosis syndrome89647000
- Maroteaux-Lamy syndrome II89647000
- Pyknodysostosis89647000
- Stanesco's dysostosis syndrome89647000
- Congenital abnormal fusion of humerus92859003
- Congenital fused humerus92859003
- Congenital abnormal shape of humerus92915006
- Congenital misshapen humerus92915006
- Congenital abnormal shape of radius92942007
- Congenital misshapen radius92942007
- Lethal Kniest-like syndrome93132001
- Congenital hypoplasia of fibula93256009
- Congenital short fibula93256009
- Congenital hypoplasia of tibia93298007
- Congenital short tibia93298007
- Congenital hypoplasia of ulna93300007
- Congenital short ulna93300007
- Dyssegmental dysplasia - Rolland-Desbuquois type95243004
- Rolland-Debuqois syndrome95243004
- Dysostosis109420003
- Congenital undergrowth of foot128061008
- Longitudinal deficiency of foot128061008
- Humeroulnar synostosis205330003
- Mesomelic dysplasia205473008
- Metachondromatosis205481009
- Chronic deafness232325008
- Aluminium bone disease236547007
- Aluminium-related osteopathy236547007
- Aluminum bone disease236547007
- Aluminum-related osteopathy236547007
- Aluminium-related fracturing osteodystrophy236549005
- Aluminum-related fracturing osteodystrophy236549005
- Idiopathic hypoparathyroidism237654002
- Canities247564004
- White forelock247564004
- Spondylodysplasia, San Diego type254046002
- Spondylodysplasia, Torrance type254047006
- Spondylodysplasia, Luton type254048001
- Boomerang dysplasia254054000
- Atelosteogenesis de la Chapelle type254055004
- Atelosteogenesis type 2254055004
- Pseudodiastrophic dysplasia254058002
- Kniest-Stickler dysplasia254059005
- Progressive pseudorheumatoid dysplasia254065005
- Immuno-osseous dysplasia254067002
- Spondyloenchondrodysplasia254079002
- Epiphyseal dysplasia254080004
- Metaphyseal anadysplasia254085009
- Dysplasias with significant membranous bone involvement254094003
- Kyphomelic dysplasia254096001
- Stuve-Wiedemann dysplasia254097005
- Multiple dislocations with dysplasia254098000
- Desbuquois dysplasia254099008
- Desbuquois syndrome254099008
- Osteodysplastic primordial dwarfism254101001
- Bruck syndrome254113006
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Dysplasia with increased bone density254120004
- Dysosteosclerosis254123002
- Endosteal hyperostoses254130008
- Endosteal hyperostoses with cerebellar hypoplasia254132000
- Familial hypertrophic osteoarthropathy254133005
- Pachydermoperiostosis - familial254133005
- Disorganised development of cartilaginous and fibrous components of the skeleton254140006
- Disorganized development of cartilaginous and fibrous components of the skeleton254140006
- Osteoglophonic dwarfism254144002
- Osteoglophonic dysplasia254144002
- Idiopathic osteolyses254147009
- Hereditary acroosteolysis254148004
- Carpal-tarsal osteolysis with nephropathy254149007
- Congenital anomalies of elbow and upper arm268265008
- Congenital enchondromatosis268274005
- Dyschondroplasia268274005
- Enchondromatosis268274005
- Multiple enchondromata268274005
- Ollier disease268274005
- Ollier's disease268274005
- Congenital exostosis268276007
- Deformity of radius271087004
- Spondylodysplastic group278708009
- Bent bone dysplasia group278832007
- Craniometadiaphyseal dysplasia278833002
- Acromesomelic dysplasia Hunter-Thompson type389167007
- Hunter-Thompson dysplasia389167007
- Precocious osteodysplasty389170006
- Yunis-Varon dysplasia389171005
- Osteoplastic dysplasia389191003
- Osteodysplastic dysplasia, type I389193000
- Osteodysplastic dysplasia, type II389195007
- Bone fragility, craniosynostosis, proptosis, hydrocephalus syndrome389199001
- Cole Carpenter syndrome389199001
- Cole-Carpenter dysplasia389199001
- Mixed sclerosing bone dysplasia389207000
- Neonatal osteosclerotic dysplasia389236000
- Blomstrand dysplasia389237009
- Lethal osteosclerotic bone dysplasia389239007
- Osteosclerotic bone dysplasia389239007
- Raine dysplasia389239007
- Raine syndrome389239007
- Lethal chondrodysplasia with fragmented bone389260001
- Dappled diaphyseal dysplasia389262009
- Genochondromatosis389264005
- Carpotarsal osteochondromatosis389272007
- Maroteaux Le-Merrer Bensahel syndrome389272007
- Whyte Hemingway carpal tarsal phalangeal osteolyses389274008
- Giacci familial neurogenic acroosteolysis389275009
- Bowing of upper limb449713008
- Nasu-Hakola disease702347001
- PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy702347001
- PLOSL - polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy702347001
- Polycystic lipomembranous osteodysplasia with sclerosing leucoencephalopathy702347001
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy702347001
- Presenile dementia with bone cysts702347001
- Dappled metaphysis syndrome702350003
- SEMD - spondyloepimetaphyseal dysplasia, Strudwick type702350003
- Spondyloepimetaphyseal dysplasia, Strudwick type702350003
- Strudwick syndrome702350003
- Congenital scoliosis with unilateral unsegmented bar702351004
- Congenital synspondylism702351004
- Spondylocarpotarsal synostosis syndrome702351004
- Vertebral fusion with carpal coalition702351004
- Autosomal recessive Larsen syndrome702400006
- Humero-spinal dysostosis702400006
- Spondyloepiphyseal dysplasia with congenital joint dislocations702400006
- Spondyloepiphyseal dysplasia, Omani type702400006
- Combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia703523004
- Roifman-Costa syndrome703523004
- Roifman-Melamed syndrome703523004
- Spondyloenchondrodysplasia with immune dysregulation703523004
- Gurrieri Sammito Bellussi syndrome715428003
- Skeletal dysplasia with epilepsy and short stature syndrome715428003
- Mesomelic dysplasia with cleft palate and camptodactyly syndrome715471007
- Reardon Hall Slaney syndrome715471007
- Mesomelic dwarfism Reinhardt-Pfeiffer type715472000
- Mesomelic dysplasia of hypoplastic ulna and fibula type715472000
- Reinhardt Pfeiffer mesomelic dysplasia715472000
- Reinhardt Pfeiffer syndrome715472000
- Rhizomelic dysplasia Patterson Lowry type715505002
- Rhizomelic dysplasia of Patterson Lowry type715505002
- Anterior bowing of legs with dwarfism715532007
- Weismann Netter syndrome715532007
- Gnathodiaphyseal dysplasia715568002
- Gnathodiaphyseal dysplasia syndrome715568002
- Mesomelic dysplasia Savarirayan type715652002
- Mesomelic dysplasia with absent fibula and triangular tibia715652002
- Spondylo-ocular syndrome715653007
- Spondyloocular syndrome715653007
- Autosomal recessive multiple epiphyseal dysplasia715672007
- Multiple epiphyseal dysplasia type 4715672007
- Multiple epiphyseal dysplasia type 1715673002
- Polyepiphyseal dysplasia type 1715673002
- Multiple epiphyseal dysplasia type 5715674008
- Polyepiphyseal dysplasia type 5715674008
- Smith McCort dysplasia715862006
- Chitty Hall Baraitser syndrome716238003
- Deafness with epiphyseal dysplasia and short stature syndrome716238003
- Acromesomelic dysplasia Maroteaux type718559000
- Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome719205008
- Camera syndrome719258003
- Pyknoachondrogenesis719258003
- Spondylometaphyseal dysplasia Algerian type719304005
- Spondylometaphyseal dysplasia Schmidt type719304005
- Spondylometaphyseal dysplasia with severe genu valgum719304005
- Kantaputra mesomelic dysplasia719397009
- Mesomelic dysplasia Kantaputra type719397009
- Mesomelic dysplasia Thai type719397009
- Lethal recessive chondrodysplasia719404009
- Maroteaux Stanescu Cousin syndrome719404009
- Leucoencephalopathy with metaphyseal chondrodysplasia syndrome719405005
- Leukoencephalopathy with metaphyseal chondrodysplasia syndrome719405005
- Cleidorhizomelic syndrome719471002
- Rhizomelic shortness with clavicular defect719471002
- Wallis Zieff Goldblatt syndrome719471002
- X-linked dominant chondrodysplasia Chassaing Lacombe type719837003
- Acrocapitofemoral dysplasia720416007
- Acropectorovertebral dysplasia720457000
- F syndrome720457000
- Craniofrontonasal dysplasia with Poland anomaly syndrome720757001
- Webster Deming syndrome720757001
- ASPED - angel-shaped phalango-epiphyseal dysplasia720984008
- Angel-shaped phalango-epiphyseal dysplasia720984008
- Angel-shaped phalangoepiphyseal dysplasia720984008
- Dacryocystitis and osteopoikilosis syndrome721082002
- Gunal Seber Basaran syndrome721082002
- Deafness, genital anomaly, metacarpal and metatarsal synostosis syndrome721086004
- Pfeiffer Kapferer syndrome721086004
- Diaphanospondylodysostosis721094006
- Epiphyseal dysplasia, microcephalus, nystagmus syndrome721975004
- Lowry Wood syndrome721975004
- Gracile bone dysplasia722109008
- Osteocraniosplenic syndrome722109008
- Osteocraniostenosis722109008
- Epiphyseal stippling with osteoclastic hyperplasia syndrome722127006
- Pacman dysplasia722127006
- EE - epileptic encephalopathy723125008
- Epileptic encephalopathy723125008
- ECO (endocrine-cerebro-osteodysplasia) syndrome723309006
- ECO syndrome723309006
- Endocrine cerebroosteodysplasia syndrome723309006
- Endocrine-cerebro-osteodysplasia syndrome723309006
- Microcephalic osteodysplastic dysplasia Saul Wilson type723404002
- Terminal osseous dysplasia and pigmentary defect syndrome723578001
- Grant syndrome723827003
- Schimke immuno-osseous dysplasia723995003
- Schimke immunoosseous dysplasia723995003
- Schimke syndrome723995003
- RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia) syndrome723999009
- RHYNS syndrome723999009
- Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome723999009
- Benign osteogenic neoplasm of bone of limb724577001
- Craniometadiaphyseal dysplasia wormian bone type725099009
- Atelosteogenesis type 1725141006
- Atelosteogenesis type I725141006
- Giant cell chondrodysplasia725141006
- Atelosteogenesis type 3725142004
- Atelosteogenesis type III725142004
- Omodysplasia725164008
- Autosomal dominant omodysplasia725165009
- Omodysplasia 2725165009
- Autosomal recessive omodysplasia725166005
- Micromelic dysplasia, dislocation of radius syndrome725166005
- Omodysplasia 1725166005
- CHST3-related skeletal dysplasia725417001
- Carbohydrate sulfotransferase 3 related skeletal dysplasia725417001
- Spondyloepiphyseal dysplasia with congenital joint dyslocations CHST3 type725417001
- Microcephalic osteodysplastic primordial dwarfism Taybi Linder type725461009
- Microcephalic osteodysplastic primordial dwarfism types I and III725461009
- Primordial microcephalic dwarfism Crachami type725461009
- Taybi Linder syndrome725461009
- Genochondromatosis type 2725904009
- Autosomal recessive lethal chondrodysplasia round femoral inferior epiphysis type732249002
- Bone dysplasia lethal Holmgren type732249002
- Melhem Fahl syndrome732263008
- Battaglia Neri syndrome733031004
- Epilepsy, microcephaly, skeletal dysplasia syndrome733031004
- Velo-facial-skeletal syndrome763616002
- Velofacioskeletal syndrome763616002
- Larsen-like syndrome B3GAT3 type763778003
- Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type763778003
- Multiple joint dislocations, short stature, craniofacial dysmorphism, congenital heart defects syndrome763778003
- SHOX (short stature homeobox) related short stature763868006
- SHOX-related short stature763868006
- Short stature homeobox related short stature763868006
- Multiple epiphyseal dysplasia with severe proximal femoral dysplasia763893008
- Colobomatous microphthalmia, rhizomelic dysplasia syndrome764942005
- Microphthalmia, coloboma, rhizomelic skeletal dysplasia764942005
- Larsen-like osseous dysplasia, short stature syndrome764956007
- Multiple epiphyseal dysplasia due to collagen 9 anomaly766717008
- Multiple epiphyseal dysplasia with miniepiphyses766750008
- Epiphyseal dysplasia, hearing loss, dysmorphism syndrome766870005
- Finucane Kurtz Scott syndrome766870005
- Multiple epiphyseal dysplasia Lowry type768935003
- Multiple epiphyseal dysplasia with Robin phenotype768935003
- Metaphyseal chondrodysplasia Kaitila type770909004
- Rhizomelic syndrome Urbach type770948004
- DSS - disproportionate short stature772086000
- Disproportionate short stature772086000
- Familial osteodysplasia Anderson type773278003
- Lethal occipital encephalocele, skeletal dysplasia syndrome773672007
- FGFR2-related bent bone dysplasia778008009
- Fibroblast growth factor receptor 2-related bent bone dysplasia778008009
- Perinatal lethal bent bone dysplasia778008009
- X-linked osteoporosis with fractures782785002
- X-linked calvarial hyperostosis782786001
- Mixed sclerosing bone dystrophy with extra-skeletal manifestation783723003
- OPD (otopalatodigital) spectrum disorder784010006
- Otopalatodigital syndrome spectrum disorder784010006
- Osteopathia striata, pigmentary dermopathy, white forelock syndrome787408008
- Whyte Murphy syndrome787408008
- Lethal congenital SLSS (short limb short stature)926342004
- Lethal congenital disproportionate short limbed short stature926342004
- Lethal congenital short limb short stature926342004
- Genochondromatosis type 11003427004
- Agenesis of fibula1003546000
- Mesomelic dysplasia of upper limb1010609002
- Congenital dysplasia of radius1142185008
- Congenital hypoplasia of bone of forearm1145430008
- Congenital hypoplasia of bone of radius and/or ulna1145430008
- Aplasia of fibula1145459008
- LRP5-related primary osteoporosis1169364005
- Low density lipoprotein receptor-related protein 5 related primary osteoporosis1169364005
- Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome1177173001
- MYSM1 (Myb like, SWIRM and MPN domains 1) deficiency1177173001
- MYSM1 deficiency1177173001
- EXTL3 (exostosin like glycosyltransferase 3) related neuro-immuno-skeletal dysplasia syndrome1177175008
- EXTL3-related neuro-immuno-skeletal dysplasia syndrome1177175008
- Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 (exostosin like glycosyltransferase 3) deficiency1177175008
- Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 deficiency1177175008
- Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome1177175008
- Lethal skeletal dysplasia, fetal akinesia, contractures, thoracic dysplasia, pulmonary hypoplasia syndrome1179299005
- Lethal skeletal dysplasia, foetal akinesia, contractures, thoracic dysplasia, pulmonary hypoplasia syndrome1179299005
- NEK9-related lethal skeletal dysplasia1179299005
- NIMA related kinase 9 lethal skeletal dysplasia1179299005
- MSBD (mixed sclerosing bone dystrophy) syndrome1197053003
- Melorheostosis with osteopoikilosis1197053003
- Mixed sclerosing bone dystrophy1197053003
- MOPD (microcephalic osteodysplastic primordial dwarfism) type II1208348002
- Majewski osteodysplastic primordial dwarfism type II1208348002
- Microcephalic osteodysplastic primordial dwarfism type II1208348002
- Glutamine rich 1-related intellectual disability, chondrodysplasia syndrome1220568003
- QRICH1-related intellectual disability, chondrodysplasia syndrome1220568003
- Ververi Brady syndrome1220568003
- Early-onset calcifying leucoencephalopathy, skeletal dysplasia1222661007
- Early-onset calcifying leukoencephalopathy, skeletal dysplasia1222661007
- Complex lethal osteochondrodysplasia1228858000
- Complex lethal osteochondrodysplasia Symoens Barnes Gistelinck type1228858000
- Isolated osteopoikilosis1231182008
- Syndromic nanophthalmos due to Kenny-Caffey syndrome1231626009
- Osteofibrous dysplasia1234828008
- Myelodysplastic neoplasm with low blasts1260268001
- Myelodysplastic syndrome with low blasts1260268001
- Refractory neutropenia1260268001
- Liberfarb syndrome1284851009
- Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome1284851009
- CANT1-related multiple epiphyseal dysplasia1363114004
- EDM7 - epiphyseal dysplasia multiple 71363114004
- MED7 - multiple epiphyseal dysplasia type 71363114004
- Multiple epiphyseal dysplasia type 71363114004
- Mesomelic dysplasia, digital anomalies, intellectual disability syndrome1363286000
- Body height below reference range1363478003
- Dysplastic cortical hyperostosis1363579009
- Dysplastic cortical hyperostosis Kozlowski Tsuruta type1363583009
- Kozlowski Tsuruta syndrome1363583009
- Dysplastic cortical hyperostosis Al-Gazali type1363584003
Frequently Asked Questions
What is ICD-10 code Q78.8?
ICD-10-CM code Q78.8 represents "Other specified osteochondrodysplasias". It is a billable/specific code that can be used on a claim.
Is Q78.8 a billable code?
Yes, Q78.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q78.8 in?
Q78.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q78.8 map to?
Q78.8 maps to 212 SNOMED CT concepts: 720984008, 720416007, 66758006, 389167007, 718559000, and 207 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q78.8?
Q78.8 is linked to 2 UMLS Concept Unique Identifiers: C0029455, C0478078. 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.