Q75.2
BillableHypertelorism
Hypertelorism
Status
Billable / Specific
Parent Code
Q75Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- congenital malformation of face NOS (Q18.-)
- congenital malformation syndromes classified to Q87.-
- dentofacial anomalies [including malocclusion] (M26.-)
- musculoskeletal deformities of head and face (Q67.0-Q67.4)
- skull defects associated with congenital anomalies of brain such as:
- anencephaly (Q00.0)
- encephalocele (Q01.-)
- hydrocephalus (Q03.-)
- microcephaly (Q02)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
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
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.
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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.