2024 ICD-10-CM Diagnosis Code Q89.7

Multiple congenital malformations, not elsewhere classified

ICD-10-CM Code:
Q89.7
ICD-10 Code for:
Multiple congenital malformations, not elsewhere classified
Is Billable?
Yes - Valid for Submission
Chronic Condition Indicator: [1]
Chronic
Code Navigator:

Code Classification

  • Congenital malformations, deformations and chromosomal abnormalities
    (Q00-Q99)
    • Other congenital malformations
      (Q80-Q89)
      • Other congenital malformations, not elsewhere classified
        (Q89)

Q89.7 is a billable diagnosis code used to specify a medical diagnosis of multiple congenital malformations, not elsewhere classified. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024. The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals.

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • Acephalobrachius
  • ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder
  • Akinesia
  • Autositic twin of asymmetrical conjoined twins
  • Cantu's syndrome
  • CK syndrome
  • Cloverleaf skull syndrome
  • Cloverleaf skull with multiple congenital anomalies syndrome
  • Complex craniosynostosis
  • Congenital complete absence of upper limb
  • Congenital generalized hypercontractile muscle stiffness syndrome
  • Duhamel's syndrome
  • Ectrodactyly-ectodermal dysplasia-clefting syndrome
  • Ethmocephalus
  • Fetus with hereditary disease
  • Hydrolethalus syndrome
  • Lethal multiple pterygium syndrome
  • Male emopamil-binding protein disorder with neurological defect
  • Monocephalus
  • Monocephalus tripus dibrachius
  • Moore-Federman syndrome
  • Multiple congenital anomalies, hypotonia, seizures syndrome
  • Multiple congenital anomalies, hypotonia, seizures syndrome type 2
  • Multiple malformation syndrome with unusual brain and/or neuromuscular findings
  • Multiple pterygium syndrome
  • Native American myopathy
  • Ochoa syndrome
  • Omocephalus
  • Pentalogy of Cantrell
  • Synotus
  • Timothy syndrome
  • Timothy syndrome type 2

Clinical Classification

Clinical Information

  • Pentalogy of Cantrell

    rare congenital deformity syndrome characterized by a combination of five anomalies as a result of neural tube defect. the five anomalies are a midline supraumbilical abdominal wall defect (e.g., omphalocele), a lower sternum defect, a congenital intracardiac defect, an anterior diaphragm defect, and a diaphragmatic pericardium defect (e.g., pericardial effusion). variants with incomplete and variable combinations of the defects are known. ectopia cordis; cleft lip; and cleft palate are often associated with the syndrome.
  • Pentalogy of Cantrell

    a rare syndrome characterized by the presence of omphalocele, anterior diaphragmatic hernia, sternal cleft, ectopia cordis, and ventricular septal defect or left ventricle diverticulum.
  • Akinesia

    lack of movement.
  • Fetal Akinesia Deformation Sequence|FADS|Pena-Shokeir syndrome, Type 1

    a condition characterized by fetal akinesia and intrauterine growth restriction, that may be associated with mutation(s) in the rapsn or dok7 genes, encoding 43 kda receptor-associated protein of the synapse and protein dok-7, respectively.
  • Lethal Multiple Pterygium Syndrome

    a rare variant of multiple pterygium syndrome, characterized by severe athrogryposis, pterygium, akinesia and often hydrops fetalis and cystic hygroma. this variant is fatal, usually during the second or third trimester of pregnancy.

Tabular List of Diseases and Injuries

The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.


Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • Multiple congenital anomalies NOS
  • Multiple congenital deformities NOS

Type 1 Excludes

Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
  • congenital malformation syndromes affecting multiple systems Q87

Index to Diseases and Injuries References

The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).

Present on Admission (POA)

Q89.7 is exempt from POA reporting - The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement. Review other POA exempt codes here.

CMS POA Indicator Options and Definitions

POA IndicatorReason for CodeCMS will pay the CC/MCC DRG?
YDiagnosis was present at time of inpatient admission.YES
NDiagnosis was not present at time of inpatient admission.NO
UDocumentation insufficient to determine if the condition was present at the time of inpatient admission.NO
WClinically undetermined - unable to clinically determine whether the condition was present at the time of inpatient admission.YES
1Unreported/Not used - Exempt from POA reporting. NO

Convert Q89.7 to ICD-9-CM

  • ICD-9-CM Code: 759.7 - Mult congen anomal NEC

Code History

  • FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
  • FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
  • FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
  • FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.