Q89.7
BillableMultiple congenital malformations, not elsewhere classified
Multiple congenital malformations, not elsewhere classified
Status
Billable / Specific
Parent Code
Q89Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Multiple congenital anomalies NOS
- Multiple congenital deformities NOS
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- congenital malformation syndromes affecting multiple systems (Q87.-)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Monocephalus tripus dibrachius3680009
- Omocephalus30526003
- Akinesia33994004
- Monocephalus39564008
- EEC - Ectodermal dysplasia with ectrodactyly and cleft lip or palate39788007
- EEC syndrome39788007
- Ectodermal dysplasia with ectrodactyly and cleft lip or palate39788007
- Ectrodactyly-ectodermal dysplasia-clefting syndrome39788007
- Rudiger's syndrome39788007
- Duhamel syndrome49096008
- Duhamel's syndrome49096008
- Tondury-Duhamel anomalad49096008
- Ethmocephalus55709000
- Ethmocephaly55709000
- Lethal multiple pterygium syndrome60192008
- Multiple malformation syndrome with unusual brain and/or neuromuscular findings64162006
- Familial dwarfism AND stiff joints72913007
- Moore-Federman syndrome72913007
- Synotia77471004
- Synotus77471004
- Autosite of asymmetrical conjoined twins90313000
- Autositic twin of asymmetrical conjoined twins90313000
- Lambdoid craniosynostosis109417006
- Parieto-occipital craniosynostosis109417006
- Interparietal craniosynostosis109418001
- Sagittal craniosynostosis109418001
- Sagittal synostosis109418001
- Scaphocephaly109418001
- Fetal hereditary disease199531009
- Fetus with hereditary disease199531009
- Foetus with hereditary disease199531009
- Hereditary disorder of fetus199531009
- Amelia of upper limb205306000
- Congenital complete absence of upper limb205306000
- Transverse deficiency of arm, shoulder level205306000
- Multiple pterygium syndrome205819008
- Acephalobrachius205835001
- Ochoa syndrome236533008
- Cantu syndrome239087008
- Cantu's syndrome239087008
- Clover leaf skull deformity254022009
- Cloverleaf skull syndrome254022009
- Kleeblattschadel deformity254022009
- Pentalogy of Cantrell281587000
- Cloverleaf skull with multiple congenital anomalies syndrome717771007
- Timothy syndrome type 2719907006
- Hydrolethalus syndrome721232000
- Congenital myopathy, cleft palate. malignant hyperthermia syndrome723439002
- Native American myopathy723439002
- ADNP-related multiple congenital anomalies, intellectual disability, autism spectrum disorder766824003
- Activity dependent neuroprotector homeobox related multiple congenital anomalies, intellectual disability, autism spectrum disorder766824003
- Helsmoortel-van der Aa syndrome766824003
- CK syndrome773329005
- X-linked intellectual disability, microcephaly, cortical malformation, thin habitus syndrome773329005
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 2773643006
- Multiple congenital anomalies, hypotonia, seizures syndrome type 2773643006
- MEND (male emopamil-binding protein disorder with neurological defect) syndrome782739000
- Male EBP (emopamil-binding protein) disorder with neurological defect782739000
- Male emopamil-binding protein disorder with neurological defect782739000
- Congenital disorder of glycosylation due to PIGN (phosphatidylinositol glycan anchor biosynthesis class N) deficiency785303004
- Multiple congenital anomalies, hypotonia, seizures syndrome785303004
- PIGN-CDG - phosphatidylinositol glycan anchor biosynthesis class N congenital disorder of glycosylation785303004
- Congenital generalised hypercontractile muscle stiffness syndrome1174000008
- Congenital generalized hypercontractile muscle stiffness syndrome1174000008
- Long QT syndrome type 81230096008
- Timothy syndrome1230096008
- SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome1300119004
- SETD2 (SET domain containing 2, histone lysine methyltransferase) related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome1300119004
- SETD2-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome1300119004
- Complex craniosynostosis8611000119100
UMLS
- ABNORM MULTIPLEC0000772
- Abnormalities, MultipleC0000772
- Anomalies congenital multipleC0000772
- Anomaly congenital multiple (NOS)C0000772
- MULTIPLE ABNORMC0000772
- Malformations multipleC0000772
- Multiple AbnormalitiesC0000772
- Multiple Congenital AnomaliesC0000772
- Multiple congenital abnormalitiesC0000772
- Multiple congenital anomaliesC0000772
- Multiple congenital anomalies NOSC0000772
- Multiple congenital deformities NOSC0000772
- Multiple congenital malformationsC0000772
- abnormalities congenital multipleC0000772
- anomalies multipleC0000772
- multiple congenital anomaliesC0000772
- multiple congenital anomalyC0000772
- Multiple congenital malformations, not elsewhere classifiedC0495643
Frequently Asked Questions
What is the ICD-10 code for multiple congenital malformations, not elsewhere classified?
The ICD-10-CM code for multiple congenital malformations, not elsewhere classified is Q89.7. The full clinical description is "Multiple congenital malformations, not elsewhere classified". Q89.7 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q89.7 mean?
ICD-10-CM code Q89.7 represents "Multiple congenital malformations, not elsewhere classified". 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 Q89.7 a billable code?
Yes, Q89.7 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q89.7 in?
Q89.7 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q89.7?
Q89.7 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital malformation syndromes affecting multiple systems (Q87.-).
What SNOMED CT codes does Q89.7 map to?
Q89.7 maps to 35 SNOMED CT concepts: 766824003, 205835001, 33994004, 205306000, 90313000, and 30 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q89.7?
Q89.7 is linked to 2 UMLS Concept Unique Identifiers: C0000772, C0495643. 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.