Q77.8
BillableOth 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
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
- Achondrogenesis2391001
- Carpus curvus4530000
- Madelung deformity4530000
- Madelung's deformity4530000
- Leri-Weill dyschondrosteosis17818006
- Leri-Weill syndrome17818006
- Metatropic dwarf22764001
- Metatropic dwarfism22764001
- Metatropic dwarfism syndrome22764001
- Metatropic dysplasia22764001
- Metatropic dysplasia group22764001
- Homozygous Leri-Weill dyschondrosteosis syndrome38494008
- Homozygous dyschondrosteosis38494008
- Langer mesomelic dysplasia syndrome38494008
- Mesomelic dysplasia - Langer type38494008
- Congenital longitudinal deficiency lower limb66078008
- Congenital shortening of leg66078008
- Congenital undergrowth of lower limb66078008
- Congenital undergrowth of whole of lower limb66078008
- Hemimelia of lower limb66078008
- Longitudinal deficiency of lower limb66078008
- Campomelic dysplasia74928006
- Campomelic dysplasia with autosomal sex reversal74928006
- Camptomelic dysplasia74928006
- Leg reduction deformity77595004
- Reduction deformity of lower limb77595004
- Congenital undergrowth of foot128061008
- Longitudinal deficiency of foot128061008
- Lethal retarded ossification syndromes205482002
- Trident hand249755001
- Schneckenbecken dysplasia254049009
- Epiphyseal dysplasia, multiple, with early onset diabetes mellitus254066006
- Wolcott-Rallison dysplasia254066006
- Wolcott-Rallison syndrome254066006
- Acromicric dysplasia254090007
- Bent bone dysplasia group278832007
- Acromesomelic dwarfism279082008
- Acromesomelic dysplasia279082008
- Acromesomelic dysplasia group279082008
- Acromesomelic dysplasia syndrome279082008
- Lethal chondrodysplasia with fragmented bone389260001
- Astley-Kendall dysplasia389263004
- Brachydactylous dwarfism Mseleni type715470008
- Mseleni joint disease715470008
- Parastremmatic dwarfism722210007
- Parastremmatic dysplasia722210007
- Sharma Kapoor Ramji syndrome783004003
- Thin ribs, tubular bones, dysmorphism syndrome783004003
- Bilateral Madelung deformity890380004
- Congenital dysplasia of radius1142185008
- Overgrowth, metaphyseal undermodeling, spondylar dysplasia syndrome1169363004
- Overgrowth, metaphyseal undermodelling, spondylar dysplasia syndrome1169363004
- Body height below reference range1363478003
- Bilateral congenital dysplasia of upper limbs16009151000119103
- Congenital dysplasia of bilateral arms16009151000119103
- Congenital dysplasia of bilateral upper extremities16009151000119103
- Congenital dysplasia of bilateral upper limbs16009151000119103
- Congenital dysplasia of both upper limbs16009151000119103
- Congenital dysplasia of left arm16008831000119109
- Congenital dysplasia of left upper extremity16008831000119109
- Congenital dysplasia of left upper limb16008831000119109
- Congenital dysplasia of right arm16009071000119106
- Congenital dysplasia of right upper extremity16009071000119106
- Congenital dysplasia of right upper limb16009071000119106
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.
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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.