SED - Spondyloepiphyseal dysplasia
Congenital conductive hearing loss
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis
Spondyloepimetaphyseal dysplasia Missouri type
SED CONGENITA
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
Spondyloepimetaphyseal dysplasia with joint laxity type 3
Spondyloepimetaphyseal dysplasia PAPSS2 (3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2) type
Spondyloepimetaphyseal dysplasia 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 type
Anauxetic dysplasia
Leber's amaurosis
Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type
Longitudinal deficiency of metatarsal bone
Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome
Degenerative polyarthritis
Spondylometaphyseal dysplasia Golden type
Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type
Humero-spinal dysostosis
Brachymetatarsia of 4th metatarsal
Pseudo-Morquio syndrome type 2
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type
Spondyloepiphyseal dysplasia tarda
Chronic deafness
Short fourth metatarsal
X-linked spondyloepimetaphyseal dysplasia
Brachymetatarsia of fourth metatarsal
SEMDJL3 - spondyloepimetaphyseal dysplasia with joint laxity type 3
SED (spondyloepiphyseal dysplasia) Stanescu type
Spondyloepimetaphyseal dysplasia Irapa type
Spondyloepimetaphyseal dysplasia with joint laxity Hall type
Congenital hypoplasia of bone of radius and/or ulna
Selective tooth agenesis
Spondyloepiphyseal dysplasia Reardon type
Spondyloepiphyseal dysplasia Kimberley type
SEDc
Spondyloepiphyseal dysplasia, Omani type
Spondyloepimetaphyseal dysplasia Menger type
EVEN-plus syndrome
Congenital hypotrichosis
Spondylo-megaepiphyseal-metaphyseal dysplasia
Spondyloepiphyseal dysplasia and brachydactyly with speech disorder syndrome
Spondyloepimetaphyseal dysplasia with joint laxity type 2
Eiken syndrome
SHILCA syndrome
Hypotrichosis congenita
CRB - Congenital retinal blindness
Disproportionate short stature
Oligodontia
Spondyloepimetaphyseal dysplasia anauxetic type
DSS - disproportionate short stature
SEMDG - spondyloepimetaphyseal dysplasia Genevieve type
Multiple epiphyseal dysplasia with myopia and deafness syndrome
Spondyloepiphyseal dysplasia MacDermot type
Spondyloepiphyseal dysplasia, congenita
SEMDJL1 - spondyloepimetaphyseal dysplasia with joint laxity type 1
Spondyloepiphyseal dysplasia congenita group (disorder)
Spondyloepimetaphyseal dysplasia Handigodu type
microRNA 140-related spondyloepiphyseal dysplasia
Congenital short ulna
Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type
Abnormally short fourth metatarsal
SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA
Spondyloepiphyseal dysplasia congenita (SEDC), COL2A1-related
Tattoo dysplasia
Pseudoachondroplastic dysplasia
SEDT - Spondyloepiphyseal dysplasia tarda
Spondyloepiphyseal dysplasia congenita group
Spondyloepiphyseal dysplasia with severe brachydactyly and cone-shaped epiphyses
Spondyloperipheral dysplasia
Spondyloepimetaphyseal dysplasia type 2
Congenital hypotrichia
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
Spondyloepimetaphyseal dysplasia Isidor type
Spondyloepiphyseal dysplasia with congenital joint dislocations
Congenital retinal blindness
Multiple epiphyseal dysplasia Beighton type
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome
Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome
SEDC - Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
Czech dysplasia metatarsal type
EVEN (epiphyseal, vertebral, ear dysplasia, nose) plus associated findings syndrome
Dyggve-Melchior-Clausen syndrome
Mild spondyloepiphyseal dysplasia with early onset osteoarthritis due to collagen type II alpha 1 mutation
Spondyloepimetaphyseal dysplasia with joint laxity type 1
Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome
Multiple epiphyseal dysplasia Al-Gazali type
Spondyloepimetaphyseal dysplasia aggrecan type
Spondyloepiphyseal dysplasia Stanescu type
Autosomal recessive Larsen syndrome
Dyggve-Melchior-Clausen dysplasia
Whyte syndrome
X-linked spondylometaphyseal dysplasia
Immuno-osseous dysplasia
Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome
Scoliosis in skeletal dysplasia
Leber amaurosis
Opsismodysplasia
MIR140-related spondyloepiphyseal dysplasia
Sed, Congenital Type
Leber congenital amaurosis
Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome
Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal dysplasia matrilin-3 type
Spondyloepiphyseal dysplasia Cantu type
Spondyloepiphyseal dysplasia with joint laxity
Short stature, kyphosis, hypoplasia of basal ilia-cone epiphyses, facial dysmorphism syndrome
Mild spondyloepiphyseal dysplasia with premature onset arthrosis
Congenital hypoplasia of ulna
Multiple epiphyseal dysplasia and macrocephaly with distinctive facies syndrome
Spondyloepimetaphyseal dysplasia Genevieve type
Spondyloepimetaphyseal dysplasia Geneviève type
Spondyloepiphyseal dysplasia Nishimura type
Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
Spondyloperipheral dysplasia with short ulna syndrome
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome
Pseudoachondroplasia
SPONDYLOEPIPHYSEAL DYSPLASIA, CONGENITAL TYPE
Spondyloepimetaphyseal dysplasia with multiple dislocations
Brachymetatarsia
SED syndrome
Sponastrime dysplasia
Spondyloepiphyseal dysplasia Maroteaux type
Spondyloepiphyseal dysplasia tarda Kohn type
Congenital hypoplasia of bone of forearm
Spondyloepimetaphyseal dysplasia Shohat type
Roifman syndrome
Spondyloepimetaphyseal dysplasia with joint laxity, EXOC6B type
Spondyloepimetaphyseal dysplasia
Spondyloepimetaphyseal dysplasia Pakistani type
Cono-spondylar dysplasia
Spondyloepimetaphyseal dysplasia PAPSS2 type

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.

How does Q77.7 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like spondyloepiphyseal dysplasia 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 Q77.7?

Q77.7 maps to the ICD-11 code: LD24.3 (Spondyloepiphyseal or spondyloepimetaphyseal dysplasias).

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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.