AutoICD API

Q77.8

Billable

Oth osteochndrdys w defct of growth of tublr bones and spine

Other osteochondrodysplasia with defects of growth of tubular bones and spine

Status

Billable / Specific

Parent Code

Q77

ICD-11 Mapping

1 equivalent

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(9)
Q77.0

Achondrogenesis

BillableQ77.1

Thanatophoric short stature

BillableQ77.2

Short rib syndrome

BillableQ77.3

Chondrodysplasia punctata

BillableQ77.4

Achondroplasia

BillableQ77.5

Diastrophic dysplasia

BillableQ77.6

Chondroectodermal dysplasia

BillableQ77.7

Spondyloepiphyseal dysplasia

BillableQ77.9

Osteochndrdys w defct of grth of tublr bones and spine, unsp

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD24.ZSyndromes with skeletal anomalies as a major feature, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(130)

SNOMED CT

UMLS

Clinical Terms

  • Congenital dysplasia of left arm
  • Congenital dysplasia of left upper extremity
  • Madelung's deformity
  • Metatropic dwarfism syndrome
  • Congenital shortening of leg
  • Leri-Weill syndrome
  • Campomelic dysplasia
  • Acromesomelic dysplasia syndrome
  • Reduction deformity of lower limb
  • Epiphyseal dysplasia, multiple, with early onset diabetes mellitus
  • Metatropic dysplasia group
  • Leg reduction deformity
  • Body height below reference range
  • Congenital undergrowth of foot
  • Leri-Weill dyschondrosteosis
  • Parastremmatic dysplasia
  • Congenital undergrowth of lower limb
  • Congenital undergrowth of whole of lower limb
  • Metatropic dwarfism
  • Sharma Kapoor Ramji syndrome
  • Congenital longitudinal deficiency lower limb
  • Congenital dysplasia of right upper extremity
  • Homozygous dyschondrosteosis
  • Wolcott-Rallison syndrome
  • Bilateral congenital dysplasia of upper limbs
  • Congenital dysplasia of right upper limb
  • Congenital dysplasia of right arm
  • Langer mesomelic dysplasia syndrome
  • Congenital dysplasia of radius
  • Bent bone dysplasia group
  • Mesomelic dysplasia - Langer type
  • Metatropic dysplasia
  • Congenital dysplasia of bilateral upper limbs
  • Longitudinal deficiency of lower limb
  • Acromesomelic dysplasia
  • Longitudinal deficiency of foot
  • Mseleni joint disease
  • Lethal retarded ossification syndromes
  • Hemimelia of lower limb
  • Carpus curvus
  • Congenital dysplasia of both upper limbs
  • Acromicric dysplasia
  • Congenital dysplasia of left upper limb
  • Metatropic dwarf
  • Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome
  • Homozygous Leri-Weill dyschondrosteosis syndrome
  • Parastremmatic dwarfism
  • Astley-Kendall dysplasia
  • Lethal chondrodysplasia with fragmented bone
  • Schneckenbecken dysplasia
  • Congenital dysplasia of bilateral upper extremities
  • Overgrowth, metaphyseal undermodelling, spondylar dysplasia syndrome
  • Madelung deformity
  • Achondrogenesis
  • Congenital dysplasia of bilateral arms
  • Thin ribs, tubular bones, dysmorphism syndrome
  • Trident hand
  • Campomelic dysplasia with autosomal sex reversal
  • Acromesomelic dysplasia group
  • Brachydactylous dwarfism Mseleni type
  • Camptomelic dysplasia
  • Acromesomelic dwarfism
  • Bilateral Madelung deformity
  • Wolcott-Rallison dysplasia
Frequently Asked Questions
What is the ICD-10 code for oth osteochndrdys w defct of growth of tublr bones and spine?

The ICD-10-CM code for oth osteochndrdys w defct of growth of tublr bones and spine is Q77.8. The full clinical description is "Other osteochondrodysplasia with defects of growth of tubular bones and spine". Q77.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q77.8 mean?

ICD-10-CM code Q77.8 represents “Other osteochondrodysplasia with defects of growth of tubular bones and spine”. 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 Q77.8 a billable code?

Yes, Q77.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q77.8 in?

Q77.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q77.8?

Q77.8 has Excludes1 notes indicating codes that cannot be used together with it, including: mucopolysaccharidosis (E76.0-E76.3).

What SNOMED CT codes does Q77.8 map to?

Q77.8 maps to 28 SNOMED CT concepts: 2391001, 279082008, 254090007, 389263004, 278832007, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q77.8?

Q77.8 is linked to 1 UMLS Concept Unique Identifier: C0478077. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q77.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth osteochndrdys w defct of growth of tublr bones and spine 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 Q77.8?

Q77.8 maps to the ICD-11 code: LD24.Z (Syndromes with skeletal anomalies as a major feature, unspecified).

Automate ICD-10 Coding With AI

Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.

Try FreeView API Docs

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.