Q38.6
BillableOther congenital malformations of mouth
Other congenital malformations of mouth
Status
Billable / Specific
Parent Code
Q38Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital malformation of mouth NOS
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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Ectopic oral sebaceous glands50584008
- Ectopic sebaceous gland tissue50584008
- Ectopic sebaceous glands50584008
- Fordyce disease50584008
- Fordyce granules50584008
- Fordyce spots50584008
- Fordyce spots of mouth50584008
- Fordyce's disease50584008
- Fordyce's disease of mouth50584008
- Fordyce's granules50584008
- Gingival cyst58271001
- Gingival odontogenic cyst58271001
- Astomia91946007
- Congenital absence of mouth91946007
- Congenital anomaly of oral mucosa109434003
- Developmental anomaly of oral mucosa109434003
- Buccal bifurcation cyst109552000
- Ectopic oral gastrointestinal cyst109554004
- Heterotopic oral gastrointestinal cyst109554004
- Congenital anomaly of mouth128334002
- Congenital malformation of mouth128334002
- Cyst of oral soft tissue196546001
- Brachymesophalangia205317004
- Hyperpigmentation of oral mucosa235038002
- Melanin pigmentation of oral mucosa235038002
- Inflammatory odontogenic cyst235112000
- Congenital anomalies of tongue, mouth and pharynx253750008
- Congenital malformation of tongue, mouth and pharynx253750008
- Congenital abnormality of oral cavity282041002
- Congenital anomaly of oral cavity282041002
- Congenital malformation of oral cavity282041002
- Familial white folded mucosal dysplasia389203001
- Hereditary leukokeratosis of mucosa389203001
- Hereditary oral keratosis389203001
- Hereditary white sponge naevus389203001
- Hereditary white sponge nevus389203001
- White sponge naevus389203001
- White sponge naevus of mucosa389203001
- White sponge nevus389203001
- White sponge nevus of mucosa389203001
- Fordyce spots of lips403368002
- Fordyce spots of buccal mucosa403369005
- Hereditary mucoepithelial dysplasia403442005
- Hypertrichosis with congenital macrogingivae403532006
- CPLS - cleft palate-lateral synechia syndrome403772000
- Cleft palate lateral synechia syndrome403772000
- Syngnathia403772000
- Facial milia, lobate tongue, lingual and labial frenula syndrome403773005
- Gorlin-Psaume syndrome403773005
- Orofacial cleft449790007
- Fraenal attachment698842006
- Fraenal tag698842006
- Frenal attachment698842006
- Frenal tag698842006
- Cataract with aberrant oral frenula and growth delay syndrome715988005
- Wellesley Carman French syndrome715988005
- Oral-facial-digital syndrome Gabrielli type718681002
- Oral-facial-digital syndrome type 11718681002
- Oro-facial digital syndrome type 11718681002
- Orofaciodigital syndrome Gabrielli type718681002
- Orofaciodigital syndrome type 11718681002
- Oro-facial digital syndrome type 5722105002
- Orofaciodigital syndrome Thurston type722105002
- Orofaciodigital syndrome type 5722105002
- Thurston syndrome722105002
- Melanosis of mucosa of body orifice724847001
- Mucosal melanosis724847001
- Clayton-Smith Donnai syndrome732950006
- Ichthyosis, oral and digital anomalies syndrome732950006
- Microcephaly, cerebral malformation, orofaciodigital syndrome763837007
- Oro-facial digital syndrome type 14763837007
- Orofaciodigital syndrome type 14763837007
- Ectodermal dysplasia short stature syndrome764995008
- Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome764995008
- Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome764995008
- OFD18 - oral-facial-digital syndrome type 181177179002
- Oral-facial-digital syndrome with short stature and brachymesophalangia1177179002
- Orofaciodigital syndrome type 181177179002
UMLS
- ABNORM MOUTHC0026633
- Abnormal mouthC0026633
- Abnormalities, MouthC0026633
- Abnormality of the mouthC0026633
- Abnormality, MouthC0026633
- Congenital anomaly of mouthC0026633
- Congenital anomaly of mouth (disorder)C0026633
- Congenital malformation of mouthC0026633
- Congenital malformation of mouth NOSC0026633
- Congenital mouth malformation NOSC0026633
- Congenital oral malformationC0026633
- Congenital oral malformation NOSC0026633
- MOUTH ABNORMC0026633
- Mouth AbnormalitiesC0026633
- Mouth AbnormalityC0026633
- Other congenital malformations of mouthC0478026
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of mouth?
The ICD-10-CM code for other congenital malformations of mouth is Q38.6. The full clinical description is "Other congenital malformations of mouth". Q38.6 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q38.6 mean?
ICD-10-CM code Q38.6 represents "Other congenital malformations of mouth". 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 Q38.6 a billable code?
Yes, Q38.6 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q38.6 in?
Q38.6 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q38.6?
Q38.6 has Excludes1 notes indicating codes that cannot be used together with it, including: dentofacial anomalies (M26.-); macrostomia (Q18.4); microstomia (Q18.5).
What SNOMED CT codes does Q38.6 map to?
Q38.6 maps to 30 SNOMED CT concepts: 91946007, 205317004, 109552000, 403772000, 715988005, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q38.6?
Q38.6 is linked to 2 UMLS Concept Unique Identifiers: C0026633, C0478026. 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.