Q75.2
BillableHypertelorism
Hypertelorism
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •congenital malformation of face NOSQ18
- •congenital malformation syndromes classified toQ87
- •dentofacial anomalies [including malocclusion]M26
- •musculoskeletal deformities of head and faceQ67.0-Q67.4
- skull defects associated with congenital anomalies of brain such as:
- •anencephalyQ00.0
- •encephaloceleQ01
- •hydrocephalusQ03
- •microcephalyQ02
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(7)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(137)
SNOMED CT
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Congenital small ears35045004
- Microtia35045004
- Atresia of external auditory canal75355004
- Congenital atresia of external auditory canal75355004
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- Facial-limb disruptive spectrum89444000
- Hypoglossia-hypodactyly syndrome89444000
- Oromandibular-limb hypogenesis spectrum89444000
- Sphenoidal dysostosis109414004
- Rigid flat foot203532008
- Congenital preauricular fistula204272007
- Fistula auris congenita204272007
- Preauricular fistula204272007
- Preauricular sinus204272007
- CVT - Congenital vertical talus205082007
- Congenital vertical talus205082007
- Convex pes valgus205082007
- Rocker bottom foot205082007
- Congenital cavus foot205091006
- Congenital pes cavus205091006
- Irreducible joint dislocation239754004
- Persistent dislocation of joint239754004
- Telecanthus246803005
- Diaphragmatic hernia-exomphalos-corpus callosum agenesis702418009
- Diaphragmatic hernia-exomphalos-hypertelorism syndrome702418009
- Donnai-Barrow syndrome702418009
- Faciooculoacousticorenal syndrome702418009
- Bixler Christian Gorlin syndrome721836009
- HMC (hypertelorism, microtia, clefting) syndrome721836009
- Hypertelorism with microtia and facial clefting syndrome721836009
- Brachycephalofrontonasal dysplasia724284005
- Craniofrontonasal dysplasia Teebi type724284005
- Hypertelorism Teebi type724284005
- Teebi hypertelorism syndrome724284005
- Teebi syndrome724284005
- Charlie M syndrome733034007
- Telecanthus, hypertelorism, strabismus, pes cavus syndrome733067006
- Intellectual disability, short stature, hypertelorism syndrome771077007
- Stoll Geraudel Chauvin syndrome771077007
- HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome773667003
- Hypertelorism, preauricular sinus, punctual pits, deafness syndrome773667003
- Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome773667003
- External auditory canal atresia, vertical talus, hypertelorism syndrome783774006
- Rasmussen Johnsen Thomsen syndrome783774006
- 7q36.3 microduplication syndrome1208720000
- Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome1208720000
UMLS
- Excessive orbital separationC0020534
- Eyes wide apartC0020534
- Eyes widely setC0020534
- HYPERTELORISMC0020534
- HypertelorismC0020534
- Hypertelorism (disorder)C0020534
- Hypertelorism of OrbitC0020534
- Hypertelorism of orbitC0020534
- HypertelorismsC0020534
- Increased distance between eye socketsC0020534
- Increased distance between eyesC0020534
- Increased interpupillary distanceC0020534
- Ocular hypertelorismC0020534
- Orbital hypertelorismC0020534
- Orbital separation excessiveC0020534
- Wide-set eyesC0020534
- Widely spaced eyesC0020534
- Widely-spaced eyesC0020534
- Widened interpupillary distanceC0020534
- excessive orbital separationC0020534
- hypertelorismC0020534
- ocular hypertelorismC0020534
Clinical Terms
- Increased distance between eyes
- External auditory canal atresia, vertical talus, hypertelorism syndrome
- Eyes wide apart
- Hypertelorism (disorder)
- Ocular hypertelorism
- Preauricular fistula
- Bixler Christian Gorlin syndrome
- Persistent dislocation of joint
- Rigid flat foot
- Telecanthus
- Faciooculoacousticorenal syndrome
- Rasmussen Johnsen Thomsen syndrome
- Teebi hypertelorism syndrome
- Hypertelorism of orbit
- Congenital cavus foot
- Sphenoidal dysostosis
- Congenital preauricular fistula
- CVT - Congenital vertical talus
- Orbital separation excessive
- Congenital pes cavus
- Excessive orbital separation
- Convex pes valgus
- HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome
- Rocker bottom foot
- Wide-set eyes
- Congenital atresia of external auditory canal
- Diaphragmatic hernia-exomphalos-hypertelorism syndrome
- Preauricular sinus
- Hypertelorisms
- Telecanthus, hypertelorism, strabismus, pes cavus syndrome
- Median cleft face syndrome
- Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome
- Hypertelorism, preauricular sinus, punctual pits, hearing loss syndrome
- Fistula auris congenita
- Brachycephalofrontonasal dysplasia
- Oromandibular-limb hypogenesis spectrum
- HMC (hypertelorism, microtia, clefting) syndrome
- Widened interpupillary distance
- Hypertelorism Teebi type
- Teebi syndrome
- Facial-limb disruptive spectrum
- Charlie M syndrome
- Hypoglossia-hypodactyly syndrome
- Widely spaced eyes
- Hypertelorism with microtia and facial clefting syndrome
- Congenital small ears
- Craniofrontonasal dysplasia Teebi type
- Stoll Geraudel Chauvin syndrome
- 7q36.3 microduplication syndrome
- Diaphragmatic hernia-exomphalos-corpus callosum agenesis
- Increased distance between eye sockets
- Hypertelorism, preauricular sinus, punctual pits, deafness syndrome
- Microtia
- Intellectual disability, short stature, hypertelorism syndrome
- Orbital hypertelorism
- Congenital vertical talus
- Atresia of external auditory canal
- Increased interpupillary distance
- Irreducible joint dislocation
- Frontonasal dysplasia sequence
- Widely-spaced eyes
- Eyes widely set
- Donnai-Barrow syndrome
Frequently Asked Questions
What is the ICD-10 code for hypertelorism?
The ICD-10-CM code for hypertelorism is Q75.2. The full clinical description is "Hypertelorism". Q75.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q75.2 mean?
ICD-10-CM code Q75.2 represents “Hypertelorism”. 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 Q75.2 a billable code?
Yes, Q75.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q75.2 in?
Q75.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q75.2?
Q75.2 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital malformation of face NOS (Q18.-); congenital malformation syndromes classified to Q87.-; dentofacial anomalies [including malocclusion] (M26.-); and 6 more.
What SNOMED CT codes does Q75.2 map to?
Q75.2 maps to 21 SNOMED CT concepts: 1208720000, 75355004, 721836009, 724284005, 205082007, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q75.2?
Q75.2 is linked to 1 UMLS Concept Unique Identifier: C0020534. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q75.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypertelorism 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 Q75.2?
Q75.2 maps to the ICD-11 code: LB71.1 (Hypertelorism).
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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.