AutoICD API

Q38.5

Billable

Congenital malformations of palate, not elsewhere classified

Congenital malformations of palate, not elsewhere classified

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Congenital absence of uvula
  • Congenital malformation of palate NOS
  • Congenital high arched palate

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(134)

SNOMED CT

Clinical Terms

  • arch high palate
  • Congenital misshapen palate rugae
  • Developmental anomaly of uvula
  • Congenital malformation of palate NOS
  • Elevated palate
  • Byzanthine arch palate
  • Flat palate
  • Congenital anomaly of palatine bone
  • Congenital small palatine bone
  • High palate
  • Absence of uvula
  • Byzanthine arch palate (disorder)
  • Congenital short hard palate
  • High-arched palate
  • Oculo-palato-cerebral dwarfism
  • Oculo-palato-cerebral syndrome
  • Congenital malformation of palate
  • Ogival palate
  • Uvula aplasia
  • Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome
  • Congenital absence of uvula (disorder)
  • Congenital anomaly of palate
  • Oculopalatocerebral syndrome
  • High, arched palate
  • Palate high-arched
  • Agenesis of palatine bone
  • Persistent hyperplastic primary vitreous
  • Congenital malpositioned palate rugae
  • Agenesis of soft palate
  • Deviation of uvula
  • Absent uvula
  • Palate disorders congenital
  • high arched palate
  • Congenital misaligned palate rugae
  • Persistent foetal vasculature syndrome
  • Increased palatal height
  • Congenital malposition of palate rugae
  • Congenital abnormal shape of palatine bone
  • Persistent fetal vasculature syndrome
  • Congenital fused palatine bone
  • PHPV - persistent hyperplastic primary vitreous
  • Congenital hypoplasia of palatine bone
  • RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhoea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence
  • Absent palatine uvula
  • RAPADILINO syndrome
  • Congenital misshapen palatine bone
  • Redundant soft palate
  • Missing uvula
  • Congenital high arched palate
  • Congenital misalignment of palate rugae
  • Palate, high-arched
  • high arch palate
  • Congenital anomaly of palate (disorder)
  • Congenital absence of palatine bone
  • Congenital abnormal fusion of palatine bone
  • Congenital abnormal shape of palate rugae
  • Agenesis of uvula
  • Palatal anomalies, multiple diastemata, facial dysmorphism, developmental delay syndrome
  • Congenital anomaly of uvula
  • Palate anomalies
  • Congenital absence of uvula
  • RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence
  • Congenital absence of soft palate
Frequently Asked Questions
What is the ICD-10 code for congenital malformations of palate, not elsewhere classified?

The ICD-10-CM code for congenital malformations of palate, not elsewhere classified is Q38.5. The full clinical description is "Congenital malformations of palate, not elsewhere classified". Q38.5 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q38.5 mean?

ICD-10-CM code Q38.5 represents “Congenital malformations of palate, not elsewhere classified”. 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 Q38.5 a billable code?

Yes, Q38.5 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q38.5 in?

Q38.5 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q38.5?

Q38.5 has Excludes1 notes indicating codes that cannot be used together with it, including: dentofacial anomalies (M26.-); macrostomia (Q18.4); microstomia (Q18.5); and 2 more.

What SNOMED CT codes does Q38.5 map to?

Q38.5 maps to 23 SNOMED CT concepts: 707994006, 91901006, 1354549008, 27272007, 92870005, and 18 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q38.5?

Q38.5 is linked to 4 UMLS Concept Unique Identifiers: C0266121, C0240635, C1290576, C0869081. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q38.5 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformations of palate, not elsewhere classified 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 Q38.5?

Q38.5 maps to the ICD-11 code: LA5Z (Structural developmental anomalies of the face, 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.