2026 ICD-10-CM Diagnosis Code Q30.8Other congenital malformations of nose
ICD-10-CM Codes›Q00-Q99›Q30-Q34›Q30
- Billable — Valid for Submission
- POA Exempt
- Chronic Condition
Q30.8 is a billable ICD-10-CM diagnosis code for other congenital malformations of nose. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 154 through 156. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Respiratory congenital malformations.
Code Identity
Code Classification
Present on Admission (POA)Billing
Q30.8 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Accessory anterior naris
- Accessory nose
- Agenesis of nasal cartilages
- Cleft lip nasal deformity
- Congenital abnormal fusion of nasal bone
- Congenital abnormal fusion of vomer
- Congenital absence of nasal septum
- Congenital anomaly of nasal bone
- Congenital anomaly of nasal sinuses
- Congenital anomaly of nasal turbinate
- Congenital anomaly of vomer
- Congenital cleft nose
- Congenital deformity of nose
- Congenital deformity of wall of nasal sinus
- Congenital hypertrophy of nasal cavity
- Congenital hypoplasia of nasal cavity
- Congenital hypoplasia of nose
- Congenital malposition of nares
- Congenital malposition of nasal septum
- Congenital malposition of nasal turbinate
- Congenital malposition of nose
- Congenital perforation of the nasal sinus wall
- Congenital saddle nose
- Congenital stenosis of nasal pyriform aperture
- Cyclops
- Deformity of nasal sinus wall
- Frontonasal dysplasia sequence
- Frontonasal dysplasia with alopecia and genital anomaly syndrome
- Holoprosencephaly with nasal pyriformis aperture
- Hypoplasia and coloboma of alar cartilage with telecanthus syndrome
- Incomplete ossification of vomer
- Intellectual disability, epilepsy, bulbous nose syndrome
- Lack of ossification of vomer
- Microcornea
- Microcornea with glaucoma and absent frontal sinus syndrome
- Polyrrhinia
- Proboscis lateralis
- Prominent anterior nasal spine
- Prominent maxilla
- RAPADILINO syndrome
- Rhinocephaly
- Saddle nose
- Single naris
- Supratip dysplasia
- Telecanthus
Tabular List NotesGuidance
Coding notes and annotation back-references applicable to this code.
Inclusion Terms
- Accessory nose
- Congenital anomaly of nasal sinus wall
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- nose - Q30.8
- Anomaly, anomalous (congenital) (unspecified type) - Q89.9
- nasal sinus (wall) - Q30.8
- nose, nasal (bones) (cartilage) (septum) (sinus) - Q30.9
- specified NEC - Q30.8
- nose (acquired) (cartilage) - M95.0
- congenital - Q30.8
- sinus (wall) (congenital) - Q30.8
- nose - Q30.8
- nose - Q30.8
- Malformation (congenital) - See Also: Anomaly;
- specified type NEC - Q30.8
- nose, nasal (septum) - Q30.8
- Perforation, perforated (nontraumatic) (of)
- nasal
- congenital - Q30.8
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Accessory(congenital)
- nose
- Anomaly, anomalous(congenital) (unspecified type)
- nasal sinus (wall)
- Anomaly, anomalous(congenital) (unspecified type)
- nose, nasal (bones) (cartilage) (septum) (sinus)
- specified NEC
- Deformity
- nose (acquired) (cartilage)
- septum (acquired)
- congenital
- Deformity
- nose (acquired) (cartilage)
- sinus (wall) (congenital)
- Distortion(s) (congenital)
- nose
- Glioma(malignant)
- nose
- Malformation(congenital)
- nose
- specified type NEC
- Malposition
- congenital
- nose, nasal (septum)
- Perforation, perforated(nontraumatic) (of)
- nasal
- sinus
- congenital
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Microcornea
a congenital abnormality characterized by an abnormally small cornea. the horizontal corneal diameter is less than 10mm or less than 9mm in newborns. it is associated with an increased risk of glaucoma.Congenital Deformity of Nose
a malformation of the nose that is present at birth.
Patient EducationClinical
Birth Defects
A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.
The full article covers:
- What are birth defects?
- What causes birth defects?
- Who is at risk of having a baby with birth defects?
- How are birth defects diagnosed?
- What are the treatments for birth defects?
- Can birth defects be prevented?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert Q30.8 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q30.8Overview
Is Q30.8 (Congenital malformations of nose) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other congenital malformations of nose on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does Q30.8 group to?
When other congenital malformations of nose is the principal diagnosis on an inpatient stay, it groups to MS-DRG 154, 155, 156, with relative weights from 0.6911 to 1.5635 depending on complications. Higher weights mean higher Medicare reimbursement.
Is Q30.8 exempt from POA reporting?
Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for other congenital malformations of nose on inpatient claims.
What is the ICD-9 equivalent of Q30.8?
Under the General Equivalence Mappings, other congenital malformations of nose converts to ICD-9-CM 748.1 (nose anomaly NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
