Fordyce disease
Abnormalities, Mouth
Congenital malformation of mouth NOS
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
White sponge nevus
Brachymesophalangia
Congenital abnormality of oral cavity
Inflammatory odontogenic cyst
Congenital absence of mouth
Congenital oral malformation
White sponge naevus of mucosa
Cyst of oral soft tissue
Fordyce granules
Melanosis of mucosa of body orifice
Oral-facial-digital syndrome with short stature and brachymesophalangia
Gingival cyst
Oro-facial digital syndrome type 5
Cataract with aberrant oral frenula and growth delay syndrome
Fraenal attachment
Fordyce's granules
OFD18 - oral-facial-digital syndrome type 18
Fordyce's disease
Hypertrichosis with congenital macrogingivae
Oro-facial digital syndrome type 14
Hereditary white sponge naevus
Familial white folded mucosal dysplasia
MOUTH ABNORM
Fordyce's disease of mouth
Orofaciodigital syndrome type 11
Abnormal mouth
Gorlin-Psaume syndrome
Abnormality of the mouth
Buccal bifurcation cyst
Congenital anomaly of mouth
Ichthyosis, oral and digital anomalies syndrome
Clayton-Smith Donnai syndrome
Orofaciodigital syndrome type 14
Heterotopic oral gastrointestinal cyst
Hyperpigmentation of oral mucosa
Fordyce spots of lips
Hereditary white sponge nevus
White sponge naevus
Fordyce spots of mouth
Hereditary oral keratosis
Congenital malformation of tongue, mouth and pharynx
Congenital anomaly of oral mucosa
Orofaciodigital syndrome Thurston type
Hereditary leukokeratosis of mucosa
Orofacial cleft
Syngnathia
Ectopic oral gastrointestinal cyst
Microcephaly, cerebral malformation, orofaciodigital syndrome
Frenal attachment
Congenital anomaly of oral cavity
Facial milia, lobate tongue, lingual and labial frenula syndrome
Cleft palate lateral synechia syndrome
Ectopic oral sebaceous glands
Ectopic sebaceous glands
Congenital mouth malformation NOS
Gingival odontogenic cyst
Fordyce spots
Developmental anomaly of oral mucosa
ABNORM MOUTH
Abnormality, Mouth
Fordyce spots of buccal mucosa
Congenital anomaly of mouth (disorder)
Orofaciodigital syndrome Gabrielli type
CPLS - cleft palate-lateral synechia syndrome
Oro-facial digital syndrome type 11
Fraenal tag
Mouth Abnormalities
Wellesley Carman French syndrome
Astomia
Congenital anomalies of tongue, mouth and pharynx
Orofaciodigital syndrome type 18
Thurston syndrome
Short stature, nail dysplasia, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome
Mouth Abnormality
Frenal tag
Ectodermal dysplasia short stature syndrome
Hereditary mucoepithelial dysplasia
Congenital oral malformation NOS
White sponge nevus of mucosa
Mucosal melanosis
Congenital malformation of mouth
Congenital malformation of oral cavity
Oral-facial-digital syndrome Gabrielli type
Ectopic sebaceous gland tissue
Melanin pigmentation of oral mucosa
Oral-facial-digital syndrome type 11
Orofaciodigital syndrome type 5

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.

How does Q38.6 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of mouth 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 Q38.6?

Q38.6 maps to the ICD-11 code: LA31.Z (Structural developmental anomalies of mouth or tongue, unspecified).

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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.