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 psoriasisL40.5
- •certain conditions originating in the perinatal periodP04-P96
- •certain infectious and parasitic diseasesA00-B99
- •compartment syndrome (traumatic)A-)T79
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations, and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(8)
Also Known As / Clinical Terms(155)
SNOMED CT
- Congenital hypoplasia of breast8915006
- Hypoplasia of breast8915006
- Hypoplastic breast8915006
- Congenital webbing of neck11731003
- Neck webbing11731003
- Webbed neck11731003
- Congenital macrognathia12458006
- Congenital macrognathism12458006
- 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
Clinical Terms
- Cleft iris
- Mandibular micrognathia
- Parrot mouth
- Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome
- Congenital macrognathia
- SGFLD (splenogonadal fusion limb defect syndrome) syndrome
- Micromelus
- Retrognathia
- Brachygnathia
- Partial trisomy of chromosome 10
- Duplication of chromosome 10
- Micromelic dwarf
- Macrognathism
- Splenogonadal fusion limb defect syndrome
- 10q partial trisomy syndrome
- Bimaxillary retrusion
- Splenogonadal fusion, limb defect, micrognathia syndrome
- Cerebrocostomandibular syndrome
- Micromandible
- Mandibular condylar aplasia
- Dinno syndrome
- Micrognathism
- Congenital webbing of neck
- Neck webbing
- Aplasia of bone of upper jaw
- Macrognathia
- Agenesis of mandible
- Hypoplasia of nipple
- Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome
- Brachygnathism
- Aplasia of mandible
- Trisomy 10
- Agnathia, holoprosencephaly, situs inversus syndrome
- Acquired micrognathia
- Congenital absence of maxilla
- Congenital mandibular hypoplasia
- Congenital small mandible
- Hypoplasia of breast
- Congenital hypoplasia of mandible
- Micrognathia
- Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome
- Congenital micrognathia
- Hypoplastic breast
- Recession of bone
- Notched iris
- Distal limb deficiency with micrognathia syndrome
- Retrognathism
- Congenital macrognathism
- Agenesis of maxilla
- Congenital coloboma of iris
- Rudimentary nipple
- Mandibular condyle aplasia
- Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome
- Congenital retrognathism
- Rib gap defects with micrognathia
- Cerebro-costo-mandibular syndrome
- Micromelia
- Absent maxilla
- Graham Cox syndrome
- Splenogonadal fusion
- Autosomal dominant myopia, midfacial retrusion, sensorineural deafness, rhizomelic dysplasia syndrome
- Congenital absence of mandible
- Receding jaw
- Aplasia of maxilla
- Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
- 10q24 microduplication syndrome
- Webbed neck
- Overshot jaw
- Contractures, webbed neck, micrognathia, hypoplastic nipples syndrome
- Craniosynostosis, microretrognathia, severe intellectual disability syndrome
- Buttiens Fryns syndrome
- Nanomelia
- Mandibular micrognathism
- Small jaw
- Congenital micrognathism
- Congenital hypoplasia of breast
- Aplasia of bone of lower jaw
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: 73035005, 722429003, 249372005, 723018003, 722282008, 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.
How does M26.09 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified anomalies of jaw size affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of M26.09?
There is no direct ICD-11 mapping available for M26.09 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.