M26.09
BillableOther specified anomalies of jaw size
Other specified anomalies of jaw size
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
- Congenital hypoplasia of breast8915006
- Hypoplasia of breast8915006
- Hypoplastic breast8915006
- Congenital webbing of neck11731003
- Neck webbing11731003
- Webbed neck11731003
- Congenital macrognathism12458006
- Congenital macrognathia12458006
- Congenital hypoplasia of mandible32958008
- Congenital mandibular hypoplasia32958008
- Congenital micrognathia32958008
- Congenital micrognathism32958008
- Congenital small mandible32958008
- Mandibular micrognathia32958008
- Mandibular micrognathism32958008
- Micrognathia32958008
- Micrognathism32958008
- Micromandible32958008
- Small jaw32958008
- Cleft iris51485001
- Congenital coloboma of iris51485001
- Notched iris51485001
- Cerebro-costo-mandibular syndrome51780007
- Cerebrocostomandibular syndrome51780007
- Rib gap defects with micrognathia51780007
- Splenogonadal fusion62042001
- Brachygnathia63783001
- Brachygnathism63783001
- Overshot jaw63783001
- Parrot mouth63783001
- Receding jaw63783001
- 10q partial trisomy syndrome73035005
- Micromelia74370006
- Micromelic dwarf74370006
- Micromelus74370006
- Nanomelia74370006
- Congenital absence of mandible91896009
- Congenital absence of maxilla91897000
- Congenital retrognathism109515000
- Retrognathia109515000
- Retrognathism109515000
- Trisomy 10205651007
- Macrognathia235081004
- Macrognathism235081004
- Mandibular condylar aplasia235119009
- Mandibular condyle aplasia235119009
- Absent maxilla249372005
- Hypoplasia of nipple268290005
- Rudimentary nipple268290005
- Recession of bone298358008
- Bimaxillary retrusion699654002
- Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome722282008
- Graham Cox syndrome722282008
- Agnathia, holoprosencephaly, situs inversus syndrome722283003
- 10q24 microduplication syndrome722429003
- Buttiens Fryns syndrome722429003
- Distal limb deficiency with micrognathia syndrome722429003
- Acquired micrognathia723018003
- Duplication of chromosome 10726349006
- Partial trisomy of chromosome 10726349006
- SGFLD (splenogonadal fusion limb defect syndrome) syndrome726724005
- Splenogonadal fusion limb defect syndrome726724005
- Splenogonadal fusion, limb defect, micrognathia syndrome726724005
- Contractures, webbed neck, micrognathia, hypoplastic nipples syndrome773626008
- Dinno syndrome773626008
- Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome773626008
- Agenesis of maxilla1003558000
- Agenesis of mandible1003566009
- Aplasia of bone of lower jaw1145461004
- Aplasia of mandible1145461004
- Aplasia of bone of upper jaw1145462006
- Aplasia of maxilla1145462006
- Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome1187114007
- Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome1187114007
- Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome1229999001
- Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome1229999001
- Craniosynostosis, microretrognathia, severe intellectual disability syndrome1269224009
Frequently Asked Questions
What is the ICD-10 code for other specified anomalies of jaw size?
The ICD-10-CM code for other specified anomalies of jaw size is M26.09. The full clinical description is "Other specified anomalies of jaw size". M26.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code M26.09 mean?
ICD-10-CM code M26.09 represents "Other specified anomalies of jaw size". 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 M26.09 a billable code?
Yes, M26.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is M26.09 in?
M26.09 is in Chapter 13: Diseases of the Musculoskeletal System and Connective Tissue (codes M00-M99).
What codes cannot be used with M26.09?
M26.09 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); acromegaly (E22.0); and 1 more.
What SNOMED CT codes does M26.09 map to?
M26.09 maps to 34 SNOMED CT concepts: 12458006, 73035005, 722429003, 249372005, 723018003, and 29 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for M26.09?
M26.09 is linked to 1 UMLS Concept Unique Identifier: C0859106. 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.