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ICD-10-CM Code Q78.0
Osteogenesis imperfecta

BILLABLE
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
POA Exempt
POA Exempt Code
The Center for Medicare & Medicaid Services (CMS) requires medical coders to indicate whether or not a condition was present at the time of admission, in order to properly assign MS-DRG codes. This "Present On Admission" (POA) indicator is recorded on CMS form 4010A.
| ICD-10 from 2011 - 2016

Q78.0 is a billable ICD code used to specify a diagnosis of osteogenesis imperfecta. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

POA Indicators on CMS form 4010A are as follows:

IndicatorMeaningCMS Will Pay CC/MCC DRG Costs
YDiagnosis was present at time of inpatient admissionYes
NDiagnosis was not present at time of inpatient admissionNo
UDocumentation insufficient to determine if the condition was present at the time of inpatient admission.No
WClinically undetermined. Provider unable to clinically determine whether the condition was present at the time of inpatient admission.Yes
1Exempt from POA reportingNo


The ICD code Q780 is used to code Osteogenesis imperfecta

Osteogenesis imperfecta (OI), also known as brittle bone disease or Lobstein syndrome, is a congenital bone disorder characterized by brittle bones that are prone to fracture. OI may also present with shorter height, neurological features including communicating hydrocephalus, basilar invagination, and seizures, blue sclerae, hearing loss, or other complications. The fractures themselves can cause acute or chronic pain, reduced quality of life, and depression.

Specialty: Pediatrics, Medical Genetics, Osteology
MeSH Code: D010013
ICD 9 Code: 756.51

The classic blue sclerae of a person with osteogenesis imperfecta

Source: Wikipedia

Coding Notes for Q78.0 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
Fragilitas ossium
Osteopsathyrosis

MS-DRG Mapping

  • DRG Group #456-458 - Spinal fus except cerv with spinal curv or malig or infec or 9+ fus with MCC.
  • DRG Group #456-458 - Spinal fus except cerv with spinal curv or malig or infec or 9+ fus with CC.
  • DRG Group #456-458 - Spinal fus except cerv with spinal curv or malig or infec or 9+ fus without CC or MCC.
  • DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with MCC.
  • DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses with CC.
  • DRG Group #564-566 - Other musculoskeletal system and connective tissue diagnoses without CC or MCC.

Related Concepts SNOMET-CT

  • Osteogenesis imperfecta with blue sclerae AND dentinogenesis imperfecta (disorder)

ICD-10-CM Alphabetical Index References for 'Q78.0 - Osteogenesis imperfecta'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code Q78.0. Click on any term below to browse the alphabetical index.

Van der Hoeve(-de Kleyn) syndrome (Q78.0)
Vrolik's disease (Q78.0)
Spurway's syndrome (Q78.0)
Osteogenesis imperfecta (Q78.0)
Osteopsathyrosis(idiopathica) (Q78.0)
Lobstein(-Ekman) disease or syndrome (Q78.0)
Eddowes(-Spurway) syndrome (Q78.0)
Ekman's syndrome(brittle bones and blue sclera) (Q78.0)
Adair-Dighton syndrome(brittle bones and blue sclera, deafness) (Q78.0)

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

Osteogenesis imperfecta (exact match)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 756.51 was previously used, Q78.0 is the appropriate modern ICD10 code.


Parent Code: Q78 - Other osteochondrodysplasias

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/Q780