Q38.8
BillableOther congenital malformations of pharynx
Other congenital malformations of pharynx
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital malformation of pharynx NOS
- Imperforate pharynx
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
Related Codes(8)
Q38.0Congenital malformations of lips, not elsewhere classified
Q38.1Ankyloglossia
Q38.2Macroglossia
Q38.3Other congenital malformations of tongue
Q38.4Congenital malformations of salivary glands and ducts
Q38.5Congenital malformations of palate, not elsewhere classified
Q38.6Other congenital malformations of mouth
Q38.7Congenital pharyngeal pouch
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(97)
SNOMED CT
- Aberrant pituitary gland6537000
- Ectopic pituitary tissue6537000
- Congenital abnormality of pharynx11223009
- Congenital anomaly of pharynx11223009
- Congenital malformation of pharynx11223009
- Congenital atresia of pharynx29632002
- Imperforate pharynx29632002
- Pharyngeal atresia29632002
- Pharyngeal pituitary tissue38632003
- Congenital enlargement of nasopharynx50267003
- Facial-limb disruptive spectrum89444000
- Hypoglossia-hypodactyly syndrome89444000
- Oromandibular-limb hypogenesis spectrum89444000
- Congenital anomaly of tongue, salivary gland AND/OR pharynx105992002
- Congenital pharyngeal polyp204642008
- Incomplete closure of velopharyngeal apparatus due to anatomical abnormality229726002
- Structural velopharyngeal impairment229726002
- Velopharyngeal insufficiency229726002
- Incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction232416001
- VPI - Velopharyngeal incompetence232416001
- Velopharyngeal incompetence232416001
- Congenital anomalies of tongue, mouth and pharynx253750008
- Congenital malformation of tongue, mouth and pharynx253750008
- Congenital palato-esophageal incoordination253758001
- Congenital palato-oesophageal incoordination253758001
- Congenital palatoesophageal incoordination253758001
- Nasopharyngeal dysmotility253758001
- Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction427791009
- Congenital velopharyngeal incompetence427791009
- Congenital deformity of pharynx444667006
- Congenital incomplete closure of velopharyngeal apparatus700285006
- Congenital velopharyngeal dysfunction700285006
- Congenital velopharyngeal inadequacy700285006
- Cosack syndrome717814004
- Glossopalatine ankylosis717814004
- Imperforate oropharynx, costovertebral anomalies syndrome771185000
- Seghers syndrome771185000
- Congenital incomplete closure of velopharyngeal apparatus due to anatomical abnormality1279638007
- Congenital structural velopharyngeal impairment1279638007
- Congenital velopharyngeal anatomical insufficiency1279638007
UMLS
- Congenital abnormality of pharynxC0266120
- Congenital anomaly of pharynxC0266120
- Congenital anomaly of pharynx (disorder)C0266120
- Congenital malformation of pharynxC0266120
- Congenital malformation of pharynx NOSC0266120
- Congenital pharyngeal anomalyC0266120
- Congenital pharyngeal anomaly NOSC0266120
- Congenital atresia of pharynxC0266123
- Congenital atresia of pharynx (disorder)C0266123
- Imperforate pharynxC0266123
- Pharyngeal atresiaC0266123
- Other congenital malformations of pharynxC0478027
Clinical Terms
- Congenital velopharyngeal anatomical insufficiency
- Congenital malformation of tongue, mouth and pharynx
- VPI - Velopharyngeal incompetence
- Nasopharyngeal dysmotility
- Imperforate pharynx
- Congenital pharyngeal anomaly
- Congenital anomaly of pharynx
- Congenital pharyngeal anomaly NOS
- Congenital anomaly of tongue, salivary gland AND/OR pharynx
- Congenital anomaly of pharynx (disorder)
- Velopharyngeal incompetence
- Congenital palatoesophageal incoordination
- Congenital velopharyngeal dysfunction
- Incomplete closure of velopharyngeal apparatus due to anatomical abnormality
- Pharyngeal atresia
- Congenital abnormality of pharynx
- Structural velopharyngeal impairment
- Aberrant pituitary gland
- Congenital velopharyngeal incompetence
- Congenital anomalies of tongue, mouth and pharynx
- Velopharyngeal insufficiency
- Congenital enlargement of nasopharynx
- Glossopalatine ankylosis
- Imperforate oropharynx, costovertebral anomalies syndrome
- Congenital structural velopharyngeal impairment
- Congenital malformation of pharynx
- Congenital palato-esophageal incoordination
- Congenital atresia of pharynx
- Oromandibular-limb hypogenesis spectrum
- Pharyngeal pituitary tissue
- Congenital velopharyngeal inadequacy
- Seghers syndrome
- Facial-limb disruptive spectrum
- Congenital atresia of pharynx (disorder)
- Hypoglossia-hypodactyly syndrome
- Congenital malformation of pharynx NOS
- Ectopic pituitary tissue
- Congenital deformity of pharynx
- Cosack syndrome
- Congenital pharyngeal polyp
- Congenital incomplete closure of velopharyngeal apparatus due to anatomical abnormality
- Congenital incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction
- Incomplete closure of velopharyngeal apparatus due to neuromuscular dysfunction
- Congenital incomplete closure of velopharyngeal apparatus
- Congenital palato-oesophageal incoordination
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of pharynx?
The ICD-10-CM code for other congenital malformations of pharynx is Q38.8. The full clinical description is "Other congenital malformations of pharynx". Q38.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q38.8 mean?
ICD-10-CM code Q38.8 represents “Other congenital malformations of pharynx”. 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 Q38.8 a billable code?
Yes, Q38.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q38.8 in?
Q38.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q38.8?
Q38.8 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 Q38.8 map to?
Q38.8 maps to 18 SNOMED CT concepts: 6537000, 11223009, 253750008, 105992002, 29632002, and 13 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q38.8?
Q38.8 is linked to 3 UMLS Concept Unique Identifiers: C0266120, C0266123, C0478027. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q38.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of pharynx 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 Q38.8?
Q38.8 maps to the ICD-11 code: LB1Z (Structural developmental anomalies of the digestive tract, 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.