Accessory anterior naris
Congenital dysplasia of supratip of nose
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome
Congenital malposition of nose
Supernumerary nostril
Frontonasal dysplasia with alopecia and genital abnomality
Congenital abnormal fusion of vomer
Congenital stenosis of nasal pyriform aperture
Congenital enlarged nasal cavity
Holoprosencephaly with apertura pyriformis
Congenital saddle nose
Cornea small
Synophthalmia
Hernandez Aguirre Negrete syndrome
Median cleft face syndrome
Congenital saddle back nose
Microcornea
Cyclocephaly
Prominent maxilla
Congenital hypoplasia of nose
Congenital small nose
RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence
Congenital malposition of nasal conchae
Congenital malpositioned nasal conchae
Congenital malposition of nasal septum
Deformity of nasal sinus wall
Congenital deformity of wall of nasal sinus
Accessory nose
Proboscis lateralis
Congenital malposition of nasal turbinate
Congenital malpositioned nasal septum
Congenital abnormal fusion of nasal bone
Pyriform aperture stenosis
Unossified vomer
ALX4 (human aristaless-like 4) related frontonasal dysplasia with alopecia and genital anomaly
Cyclopia
Microcornea with glaucoma and absent frontal sinus syndrome
Congenital small nasal cavity
Frontonasal dysplasia with alopecia and genital anomaly syndrome
Congenital anomaly of nasal bone
Holoprosencephaly co-occurrent with congenital nasal pyriform aperture stenosis
Congenital swayback nose
Cleft lip nasal deformity
RAPADILINO syndrome
Accessory nostril
Congenital malformation of nose
Congenital malpositioned nose
Holoprosencephaly with nasal pyriformis aperture
Congenital perforation of the nasal sinus wall
Congenital anomaly of vomer
Congenital malpositioned naris
Congenital absence of nasal septum
Alar cartilage hypoplasia, coloboma, telecanthus syndrome
Telecanthus
Lack of ossification of vomer
Monophthalmus
Congenital hypoplasia of nasal cavity
Congenital hypoplastic nose
Craniofrontonasal dysplasia with alopecia and hypogonadism
Cyclops
Congenital cleft nose
Cleft lip with nasal deformity
Prominent anterior nasal spine
Double nose
Rhinocephaly
Synophthalmus
Polyrrhinia
Congenital malposition of nares
Congenital supratip depression of nose
Single naris
Congenital tubular nose
Congenital anomaly of nasal turbinate
Congenital deformity of nose
Congenital anomaly of nasal sinuses
Congenital supratip dorsal saddling
Frontonasal dysplasia sequence
Congenital nasal deformity
Congenital fused nasal bone
Congenital hypertrophy of nasal cavity
Incomplete ossification of vomer
Supratip dysplasia
Congenital duplication of nose
Saddle nose
Congenital fused vomer
RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhoea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence
Reduced ossification of vomer
Accessory nose (disorder)
Congenital anomaly of nasal sinus wall
Intellectual disability, epilepsy, bulbous nose syndrome
Cleft nose
Agenesis of nasal cartilages

Frequently Asked Questions

What is the ICD-10 code for other congenital malformations of nose?

The ICD-10-CM code for other congenital malformations of nose is Q30.8. The full clinical description is "Other congenital malformations of nose". Q30.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q30.8 mean?

ICD-10-CM code Q30.8 represents “Other congenital malformations of nose”. 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 Q30.8 a billable code?

Yes, Q30.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q30.8 in?

Q30.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q30.8?

Q30.8 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital deviation of nasal septum (Q67.4).

What SNOMED CT codes does Q30.8 map to?

Q30.8 maps to 45 SNOMED CT concepts: 725029001, 719163006, 1856001, 232381002, 722284009, and 40 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q30.8?

Q30.8 is linked to 3 UMLS Concept Unique Identifiers: C0265741, C2910163, C0478014. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q30.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of nose 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 Q30.8?

Q30.8 maps to the ICD-11 code: LA70.Z (Structural developmental anomalies of the nose or cavum, 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.