Q77.7
BillableSpondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia
Status
Billable / Specific
Parent Code
Q77Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- mucopolysaccharidosis (E76.0-E76.3)
Also Known As / Clinical Terms
SNOMED CT
- Pseudoachondroplasia22567005
- Pseudoachondroplastic dysplasia22567005
- Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome22567005
- SED syndrome22567005
- Brachymetatarsia30592006
- Longitudinal deficiency of metatarsal bone30592006
- SEDT - Spondyloepiphyseal dysplasia tarda51952004
- Spondyloepiphyseal dysplasia tarda51952004
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Dyggve-Melchior-Clausen dysplasia82699004
- Dyggve-Melchior-Clausen syndrome82699004
- Congenital hypoplasia of ulna93300007
- Congenital short ulna93300007
- CRB - Congenital retinal blindness193413001
- Congenital retinal blindness193413001
- Leber amaurosis193413001
- Leber congenital amaurosis193413001
- Leber's amaurosis193413001
- Scoliosis in skeletal dysplasia203661003
- Degenerative polyarthritis225655006
- Chronic deafness232325008
- Spondyloepimetaphyseal disorder254062008
- Spondyloepimetaphyseal dysplasia254062008
- Immuno-osseous dysplasia254067002
- Opsismodysplasia254068007
- SED - Spondyloepiphyseal dysplasia278713008
- SEDC - Spondyloepiphyseal dysplasia congenita278713008
- Spondyloepiphyseal dysplasia278713008
- Spondyloepiphyseal dysplasia congenita278713008
- Spondyloepiphyseal dysplasia congenita group278713008
- Mild spondyloepiphyseal dysplasia with premature onset arthrosis389159004
- Spondyloepiphyseal dysplasia with joint laxity389160009
- Sponastrime dysplasia389161008
- Spondyloperipheral dysplasia702339001
- Autosomal recessive Larsen syndrome702400006
- Humero-spinal dysostosis702400006
- Spondyloepiphyseal dysplasia with congenital joint dislocations702400006
- Spondyloepiphyseal dysplasia, Omani type702400006
- Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis715670004
- Mild spondyloepiphyseal dysplasia with early onset osteoarthritis due to collagen type II alpha 1 mutation715670004
- Spondyloepimetaphyseal dysplasia Irapa type717330004
- Spondyloepiphyseal dysplasia MacDermot type718763005
- Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome718763005
- Spondyloepiphyseal dysplasia Reardon type718764004
- Spondyloepiphyseal dysplasia Cantu type718765003
- Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome718765003
- Tattoo dysplasia718765003
- Spondyloepiphyseal dysplasia Nishimura type718766002
- Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome718766002
- Spondyloepimetaphyseal dysplasia aggrecan type719165004
- Spondyloepimetaphyseal dysplasia matrilin-3 type719166003
- Spondyloepimetaphyseal dysplasia Missouri type719171005
- Spondyloepimetaphyseal dysplasia type 2719171005
- Spondyloepimetaphyseal dysplasia 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 type719172003
- Spondyloepimetaphyseal dysplasia PAPSS2 (3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2) type719172003
- Spondyloepimetaphyseal dysplasia PAPSS2 type719172003
- Spondyloepimetaphyseal dysplasia Pakistani type719172003
- Spondyloepimetaphyseal dysplasia Shohat type719201004
- Spondyloepiphyseal dysplasia tarda Kohn type719202006
- Spondyloepiphyseal dysplasia Kimberley type719203001
- Pseudo-Morquio syndrome type 2719204007
- Spondyloepiphyseal dysplasia Maroteaux type719204007
- Multiple epiphyseal dysplasia Al-Gazali type719688002
- Multiple epiphyseal dysplasia and macrocephaly with distinctive facies syndrome719688002
- Multiple epiphyseal dysplasia Beighton type719689005
- Multiple epiphyseal dysplasia with myopia and deafness syndrome719689005
- Czech dysplasia metatarsal type720826006
- Eiken syndrome720863002
- Congenital conductive hearing loss737344003
- Spondyloepimetaphyseal dysplasia Handigodu type763885008
- Spondyloperipheral dysplasia with short ulna syndrome763886009
- Anauxetic dysplasia764460003
- Spondyloepimetaphyseal dysplasia Menger type764460003
- Spondyloepimetaphyseal dysplasia anauxetic type764460003
- Spondyloepimetaphyseal dysplasia with joint laxity Hall type766820007
- Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type766820007
- Spondyloepimetaphyseal dysplasia with joint laxity type 2766820007
- Spondyloepimetaphyseal dysplasia with multiple dislocations766820007
- Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type766820007
- Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome766821006
- Cono-spondylar dysplasia766874001
- Short stature, kyphosis, hypoplasia of basal ilia-cone epiphyses, facial dysmorphism syndrome766874001
- X-linked spondyloepimetaphyseal dysplasia770603000
- DSS - disproportionate short stature772086000
- Disproportionate short stature772086000
- Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome773300008
- Whyte syndrome773300008
- Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome773302000
- SEMDG - spondyloepimetaphyseal dysplasia Genevieve type773303005
- Spondyloepimetaphyseal dysplasia Genevieve type773303005
- Spondyloepimetaphyseal dysplasia Geneviève type773303005
- Spondylometaphyseal dysplasia Golden type773304004
- X-linked spondylometaphyseal dysplasia773304004
- Roifman syndrome773404000
- Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome773404000
- Spondylo-megaepiphyseal-metaphyseal dysplasia773693005
- Spondyloepimetaphyseal dysplasia Isidor type782821004
- Oligodontia787414001
- Selective tooth agenesis787414001
- Brachymetatarsia of 4th metatarsal890191004
- Brachymetatarsia of fourth metatarsal890191004
- Abnormally short fourth metatarsal897459007
- Short fourth metatarsal897459007
- Congenital hypoplasia of bone of forearm1145430008
- Congenital hypoplasia of bone of radius and/or ulna1145430008
- Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome1187303004
- X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome1217228004
- SED (spondyloepiphyseal dysplasia) Stanescu type1228860003
- Spondyloepiphyseal dysplasia Stanescu type1228860003
- EVEN (epiphyseal, vertebral, ear dysplasia, nose) plus associated findings syndrome1260203008
- EVEN-plus syndrome1260203008
- Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome1260203008
- SEMDJL1 - spondyloepimetaphyseal dysplasia with joint laxity type 11286833006
- Spondyloepimetaphyseal dysplasia with joint laxity Beighton type1286833006
- Spondyloepimetaphyseal dysplasia with joint laxity type 11286833006
- SEMDJL3 - spondyloepimetaphyseal dysplasia with joint laxity type 31286834000
- Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type1286834000
- Spondyloepimetaphyseal dysplasia with joint laxity type 31286834000
- Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type1286834000
- SHILCA syndrome1356736002
- Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome1356736002
- MIR140-related spondyloepiphyseal dysplasia1363285001
- Spondyloepiphyseal dysplasia with severe brachydactyly and cone-shaped epiphyses1363285001
- microRNA 140-related spondyloepiphyseal dysplasia1363285001
UMLS
- SED - Spondyloepiphyseal dysplasiaC2745959
- SED CONGENITAC2745959
- SED CongenitaC2745959
- SED congenitaC2745959
- SED, congenital typeC2745959
- SEDCC2745959
- SEDC - Spondyloepiphyseal dysplasia congenitaC2745959
- SEDcC2745959
- SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITAC2745959
- SPONDYLOEPIPHYSEAL DYSPLASIA, CONGENITAL TYPEC2745959
- Sed, Congenital TypeC2745959
- Spondyloepiphyseal Dysplasia CongenitaC2745959
- Spondyloepiphyseal dysplasiaC2745959
- Spondyloepiphyseal dysplasia congenitaC2745959
- Spondyloepiphyseal dysplasia congenita (SEDC), COL2A1-relatedC2745959
- Spondyloepiphyseal dysplasia congenita groupC2745959
- Spondyloepiphyseal dysplasia congenita group (disorder)C2745959
- Spondyloepiphyseal dysplasia, congenitaC2745959
- Spondyloepiphyseal dysplasia, congenital typeC2745959
Frequently Asked Questions
What is the ICD-10 code for spondyloepiphyseal dysplasia?
The ICD-10-CM code for spondyloepiphyseal dysplasia is Q77.7. The full clinical description is "Spondyloepiphyseal dysplasia". Q77.7 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q77.7 mean?
ICD-10-CM code Q77.7 represents "Spondyloepiphyseal dysplasia". 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 Q77.7 a billable code?
Yes, Q77.7 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q77.7 in?
Q77.7 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q77.7?
Q77.7 has Excludes1 notes indicating codes that cannot be used together with it, including: mucopolysaccharidosis (E76.0-E76.3).
What SNOMED CT codes does Q77.7 map to?
Q77.7 maps to 65 SNOMED CT concepts: 897459007, 764460003, 702400006, 30592006, 890191004, and 60 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q77.7?
Q77.7 is linked to 1 UMLS Concept Unique Identifier: C2745959. 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.