Diagnosis Code

Q77.7 SPONDYLOEPIPHYSEAL DYSPLASIA


Code Information

Diagnosis Code: Q77.7

Short Description: Spondyloepiphyseal dysplasia

Long Description: Spondyloepiphyseal dysplasia

The code Q77.7 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)
      • Osteochndrdys w defects of growth of tubular bones and spine (Q77)
        • Q77.7 Spondyloepiphyseal dysplasia

Code Version: 2022 ICD-10-CM


Synonyms

  • Brachymetatarsia
  • Brachymetatarsia of fourth metatarsal
  • Chronic deafness
  • Congenital conductive hearing loss
  • Congenital hypoplasia of ulna
  • Congenital hypotrichia
  • Cono-spondylar dysplasia
  • Czech dysplasia metatarsal type
  • Degenerative polyarthritis
  • Dyggve-Melchior-Clausen syndrome
  • Eiken syndrome
  • Immuno-osseous dysplasia
  • Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early onset osteoarthritis
  • Mild spondyloepiphyseal dysplasia with premature onset arthrosis
  • Multiple epiphyseal dysplasia Al-Gazali type
  • Multiple epiphyseal dysplasia Beighton type
  • Oligodontia
  • Opsismodysplasia
  • Osteoarthritis of multiple joints
  • Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome
  • Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
  • Roifman syndrome
  • Sponastrime dysplasia
  • Spondyloepimetaphyseal disorder
  • Spondyloepimetaphyseal dysplasia aggrecan type
  • Spondyloepimetaphyseal dysplasia anauxetic type
  • Spondyloepimetaphyseal dysplasia Genevieve type
  • Spondyloepimetaphyseal dysplasia Handigodu type
  • Spondyloepimetaphyseal dysplasia Irapa type
  • Spondyloepimetaphyseal dysplasia Isidor type
  • Spondyloepimetaphyseal dysplasia matrilin-3 type
  • Spondyloepimetaphyseal dysplasia Missouri type
  • Spondyloepimetaphyseal dysplasia PAPSS2 type
  • Spondyloepimetaphyseal dysplasia Shohat type
  • Spondyloepimetaphyseal dysplasia with joint laxity
  • Spondyloepimetaphyseal dysplasia with multiple dislocations
  • Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome
  • Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome
  • Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
  • Spondyloepiphyseal dysplasia Cantu type
  • Spondyloepiphyseal dysplasia congenita
  • Spondyloepiphyseal dysplasia Kimberley type
  • Spondyloepiphyseal dysplasia MacDermot type
  • Spondyloepiphyseal dysplasia Maroteaux type
  • Spondyloepiphyseal dysplasia Reardon type
  • Spondyloepiphyseal dysplasia Stanescu type
  • Spondyloepiphyseal dysplasia tarda
  • Spondyloepiphyseal dysplasia tarda Kohn type
  • Spondyloepiphyseal dysplasia with congenital joint dislocations
  • Spondyloepiphyseal dysplasia with joint laxity
  • Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
  • Spondylo-megaepiphyseal-metaphyseal dysplasia
  • Spondylometaphyseal dysplasia Golden type
  • Spondyloperipheral dysplasia
  • Spondyloperipheral dysplasia
  • Spondyloperipheral dysplasia with short ulna syndrome
  • X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome
  • X-linked spondyloepimetaphyseal dysplasia

Diagnostic Related Group(s)

The code Q77.7 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)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q77.7 Right Arrow 756.4 Chondrodystrophy

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
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
Q77.0 Achondrogenesis
Q77.1 Thanatophoric short stature
Q77.2 Short rib syndrome
Q77.3 Chondrodysplasia punctata
Q77.4 Achondroplasia
Q77.5 Diastrophic dysplasia
Q77.6 Chondroectodermal dysplasia
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified


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