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Q38.8

Billable

Other 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)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(97)

SNOMED CT

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.