Q30.1
BillableAgenesis and underdevelopment of nose
Agenesis and underdevelopment of nose
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital absent of nose
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(5)
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
- Congenital deformity of nose72089000
- Congenital malformation of nose72089000
- Congenital nasal deformity72089000
- Hypoplasia of eye86527000
- Rudimentary eye86527000
- Congenital absence of nasal conchae92970009
- Congenital absence of nasal turbinate92970009
- Congenital anomaly of nasal bone93011006
- Congenital anomaly of nasal turbinate93012004
- Congenital hypoplasia of nasal bone93274000
- Congenital small nasal bone93274000
- Congenital hypoplasia of nasal conchae93276003
- Congenital hypoplasia of nasal turbinate93276003
- Congenital small nasal conchae93276003
- Congenital hypoplasia of nasal septum93277007
- Congenital small nasal septum93277007
- Congenital hypoplasia of nose93278002
- Congenital hypoplastic nose93278002
- Congenital small nose93278002
- Absent nose111317000
- Agenesis of nose111317000
- Arhinia111317000
- Arrhinia111317000
- Congenital absence of nose111317000
- Underdevelopment of nose204519007
- Cleft nose204521002
- Congenital cleft nose204521002
- Telecanthus246803005
- Alar cartilage hypoplasia, coloboma, telecanthus syndrome722284009
- Hypoplasia and coloboma of alar cartilage with telecanthus syndrome722284009
- Bosma Henkin Christiansen syndrome724281002
- Bosma arhinia microphthalmia syndrome724281002
- Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome724281002
- Congenital hypoplasia of bridge of nose1144348007
- Congenital hypoplastic nasal bridge1144348007
- Congenital hypoplasia of apex of nose1144405002
- Congenital hypoplasia of nasal tip1144405002
- Hypoplastic nasal tip1144405002
UMLS
- Absent noseC0265740
- Agenesis and underdevelopment of noseC0265740
- Agenesis of noseC0265740
- Aplasia of the noseC0265740
- ArhiniaC0265740
- ArrhiniaC0265740
- Congenital absence of noseC0265740
- Congenital absence of nose (disorder)C0265740
- Congenital absence of the noseC0265740
- Failure of development of noseC0265740
- Nasal underdevelopmentC0265740
- Nose agenesiaC0265740
- Underdevelopment of noseC0265740
- Congenital absent of noseC2910162
Clinical Terms
- Arhinia
- Congenital absence of nasal conchae
- Alar cartilage hypoplasia, coloboma, telecanthus syndrome
- Telecanthus
- Hypoplasia and coloboma of alar cartilage with telecanthus syndrome
- Congenital nasal deformity
- Congenital absence of the nose
- Congenital hypoplasia of nasal conchae
- Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
- Congenital absence of nose
- Congenital absence of nasal turbinate
- Congenital small nasal septum
- Congenital hypoplastic nose
- Congenital hypoplasia of nasal turbinate
- Congenital small nasal conchae
- Absent nose
- Congenital cleft nose
- Nasal underdevelopment
- Congenital absent of nose
- Nose agenesia
- Congenital hypoplasia of nasal bone
- Bosma arhinia microphthalmia syndrome
- Congenital absence of nose (disorder)
- Aplasia of the nose
- Congenital small nasal bone
- Congenital hypoplasia of nasal tip
- Arrhinia
- Congenital anomaly of nasal bone
- Bosma Henkin Christiansen syndrome
- Failure of development of nose
- Hypoplasia of eye
- Congenital hypoplasia of bridge of nose
- Congenital hypoplasia of nose
- Congenital malformation of nose
- Congenital small nose
- Hypoplastic nasal tip
- Congenital hypoplastic nasal bridge
- Congenital anomaly of nasal turbinate
- Congenital deformity of nose
- Congenital hypoplasia of apex of nose
- Rudimentary eye
- Agenesis of nose
- Underdevelopment of nose
- Cleft nose
- Congenital hypoplasia of nasal septum
Frequently Asked Questions
What is the ICD-10 code for agenesis and underdevelopment of nose?
The ICD-10-CM code for agenesis and underdevelopment of nose is Q30.1. The full clinical description is "Agenesis and underdevelopment of nose". Q30.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q30.1 mean?
ICD-10-CM code Q30.1 represents “Agenesis and underdevelopment 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 Q30.1 a billable code?
Yes, Q30.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q30.1 in?
Q30.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q30.1?
Q30.1 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 Q30.1 map to?
Q30.1 maps to 17 SNOMED CT concepts: 111317000, 722284009, 724281002, 204521002, 92970009, and 12 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q30.1?
Q30.1 is linked to 2 UMLS Concept Unique Identifiers: C0265740, C2910162. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q30.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like agenesis and underdevelopment 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 Q30.1?
Q30.1 maps to the ICD-11 code: LA70.0 (Arrhinia).
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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.