M26.89
BillableOther dentofacial anomalies
Other dentofacial anomalies
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
- arthropathic psoriasis (L40.5-)
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- compartment syndrome (traumatic) (T79.A-)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Cheilognathoschisis77414002
- Cleft lip AND cleft jaw77414002
- Cheilognathoprosoposchisis88659005
- Oblique facial cleft to upper lip AND upper jaw88659005
- Facial-limb disruptive spectrum89444000
- Hypoglossia-hypodactyly syndrome89444000
- Oromandibular-limb hypogenesis spectrum89444000
- Congenital absence of mandible91896009
- Congenital absence of maxilla91897000
- Agnathia91922000
- Congenital absence of jaw91922000
- Cleft mandible92822004
- Mandibular cleft92822004
- Congenital abnormal fusion of mandible92865003
- Congenital fused mandible92865003
- Congenital abnormal fusion of maxilla92866002
- Congenital fused maxilla92866002
- Congenital abnormal shape of mandible92926000
- Congenital misshapen mandible92926000
- Congenital abnormal shape of maxilla92927009
- Congenital misshapen maxilla92927009
- Lack of ossification of mandible93106007
- Unossified mandible93106007
- Lack of ossification of maxilla93107003
- Unossified maxilla93107003
- Incomplete ossification of mandible93590001
- Reduced ossification of mandible93590001
- Incomplete ossification of maxilla93591002
- Reduced ossification of maxilla93591002
- Congenital anomaly of maxilla128223002
- Congenital anomaly of mandible128224008
- Soft tissue impingement196403002
- Prominent maxilla248399003
- Absent maxilla249372005
- Cheilognathopalatoschisis337471007
- Cleft upper lip, upper jaw AND palate337471007
- Facial skeletal pattern - finding366373007
- Finding of facial skeletal pattern366373007
- Congenital failure of fusion between maxillary and mandibular processes413906003
- Deformity of bone of face433096001
- Deformity of facial bone433096001
- Long lip449912005
- Long vertical length of upper lip449912005
- Short lip449913000
- Short vertical length of upper lip449913000
- Long lower third of face471397004
- Short lower third of face699439001
- Long middle third of face699440004
- Auriculo-condylar syndrome702443003
- Auriculocondylar syndrome702443003
- Dysgnathia complex702443003
- Question-mark ear syndrome702443003
- Deformity of mandibular condyle702754009
- Increased gonial angle708667008
- Decreased gonial angle708668003
- Bifid mandibular condyle708669006
- Hemimaxillofacial dysplasia708674003
- Congenital malformation of mandibular glenoid fossa708677005
- Hyperdivergent mandibular plane angle708686000
- Absence of mandibular condyle709492005
- Absent mandibular condyle709492005
- Low mandibular plane angle709496008
- Steep mandibular plane angle709997007
- Cant of occlusal plane down on left due to dental asymmetry710100004
- Atypical condylar angulation710101000
- Atypical condylar angulation of mandible710101000
- Cant of occlusal plane down on right due to dental asymmetry710102007
- Cant of occlusal plane down on left due to skeletal asymmetry710103002
- Cant of occlusal plane down on right due to skeletal asymmetry710104008
- Flat mandibular plane angle710243000
- Increased posterior face height710780005
- Deep mentolabial sulcus710781009
- Increase of chin to throat length711291005
- Decrease of chin to throat length711292003
- Hypodivergent mandibular plane angle711457008
- Increased lower face height711460001
- Decreased lower face height711461002
- Decreased posterior face height711463004
- Increased lower anterior face height711465006
- Decreased lower anterior face height711466007
- Long face height711584006
- Decreased maxillary vestibular depth714526009
- Decreased mandibular vestibule depth714527000
- Cecatto de Lima Pinheiro syndrome722062004
- Oculotrichodysplasia722062004
- Congenital absence of right mandibular condyle736781007
- Right condyle absent736781007
- Congenital absence of left mandibular condyle736782000
- Left condyle absent736782000
- Acute nasolabial angle737033000
- Obtuse nasolabial angle737034006
- Isolated congenital maxillomandibular fusion763317002
- Isolated congenital syngnathia763317002
- Shallow mentolabial sulcus767358005
- Incomplete ossification of cranium773586004
- Incomplete ossification of skull773586004
- Abnormal shape of condyloid process of mandible448981000124104
- Abnormal shape of mandibular condyle448981000124104
Frequently Asked Questions
What is the ICD-10 code for other dentofacial anomalies?
The ICD-10-CM code for other dentofacial anomalies is M26.89. The full clinical description is "Other dentofacial anomalies". M26.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M26.89 mean?
ICD-10-CM code M26.89 represents "Other dentofacial anomalies". It is classified under Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue and is a billable/specific code that can be used on a claim.
Is M26.89 a billable code?
Yes, M26.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M26.89 in?
M26.89 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M26.89?
M26.89 has Excludes1 notes indicating codes that cannot be used together with it, including: hemifacial atrophy or hypertrophy (Q67.4); unilateral condylar hyperplasia or hypoplasia (M27.8).
What SNOMED CT codes does M26.89 map to?
M26.89 maps to 68 SNOMED CT concepts: 448981000124104, 709492005, 249372005, 737033000, 91922000, and 63 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M26.89?
M26.89 is linked to 1 UMLS Concept Unique Identifier: C0477464. 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.