Q10.0
BillableCongenital ptosis
Congenital ptosis
Coding Notes
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
- •inborn errors of metabolismE70-E88
- •cleft lip and cleft palateQ35-Q37
- •congenital malformation of cervical spine, , ,Q05.0, Q05.5, Q67.5, Q76.0-Q76.4
- •congenital malformation of larynxQ31
- •congenital malformation of lip NECQ38.0
- •congenital malformation of noseQ30
- •congenital malformation of parathyroid glandQ89.2
- •congenital malformation of thyroid glandQ89.2
Related Codes(7)
Q10.1Congenital ectropion
Q10.2Congenital entropion
Q10.3Other congenital malformations of eyelid
Q10.4Absence and agenesis of lacrimal apparatus
Q10.5Congenital stenosis and stricture of lacrimal duct
Q10.6Other congenital malformations of lacrimal apparatus
Q10.7Congenital malformation of orbit
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(156)
SNOMED CT
- Ablepharia13401001
- Ablepharon13401001
- Ablepharon - absent eyelids13401001
- Open eye13401001
- Recurrent laryngeal nerve palsy42998008
- Vagus nerve laryngeal paralysis42998008
- Partial ablepharon45484000
- Myogenic blepharoptosis53279002
- Myogenic ptosis53279002
- Agenesis of iris69278003
- Aniridia69278003
- Aplasia of iris69278003
- Congenital absence of iris69278003
- Congenital aniridia69278003
- Irideraemia69278003
- Irideremia69278003
- Congenital ectopic lens74969002
- Congenital subluxation of lens74969002
- Ectopia lentis74969002
- Corectopia193523008
- Ectopia pupillae193523008
- Ectopic pupil193523008
- Lower lacrimal punctum finding246857003
- Lower lacrimal punctum observation246857003
- Congenital ptosis268163008
- Congenital ptosis of upper eyelid268163008
- Congenital myogenic blepharoptosis314508003
- Congenital myogenic ptosis314508003
- Congenital dysgenetic ptosis315297006
- Congenital ectopic pupil392461003
- Epicanthus inversus400956000
- Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Ohdo blepharophimosis syndrome412787009
- Congenital absence of lacrimal drainage structure418087009
- Dysgenesis of lacrimal punctum422731002
- BPES - blepharophimosis epicanthus inversus ptosis syndrome715391004
- Blepharophimosis epicanthus inversus ptosis syndrome715391004
- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome717914000
- Frydman Cohen Karmon syndrome717914000
- Blepharoptosis, myopia, ectopia lentis syndrome717915004
- Aniridia, ptosis, intellectual disability, familial obesity syndrome720987001
- Microbrachycephaly, ptosis, cleft lip syndrome723403008
- Richieri Costa Guion Almeida Ramos syndrome723403008
- Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome724016008
- Faulk Epstein Jones syndrome724064004
- Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome724064004
- Deletion of part of long arm of chromosome 3726370000
- McPherson Hall syndrome726619004
- Ptosis, strabismus, ectopic pupil syndrome726619004
- Conductive deafness, ptosis, skeletal anomalies syndrome763213001
- Jackson Barr syndrome763213001
- Ptosis and vocal cord paralysis syndrome771263004
- Tucker syndrome771263004
- Blepharophimosis, intellectual disability syndrome788584007
- 3q23 microdeletion syndrome890180006
- BPES (blepharophimosis epicanthus inversus ptosis syndrome) plus890180006
- Blepharophimosis epicanthus inversus ptosis syndrome plus890180006
- Metopic ridging, ptosis, facial dysmorphism syndrome1179283004
- Epicanthal fold1362054007
- Epicanthic fold1362054007
- Bilateral congenital ptosis of upper eyelids12235641000119107
- Congenital ptosis of bilateral upper eyelids12235641000119107
- Congenital ptosis of both upper eyelids12235641000119107
- Bilateral ptosis of upper eyelids346061000119101
- Ptosis of bilateral upper eyelids346061000119101
- Ptosis of both upper eyelids346061000119101
- Congenital ptosis of left upper eyelid12235681000119102
- Congenital ptosis of right upper eyelid12235721000119108
UMLS
- Congenital Eyelid PtosisC0266573
- Congenital drooping upper eyelidC0266573
- Congenital ptosisC0266573
- Congenital ptosis (disorder)C0266573
- Congenital ptosis of eyelidC0266573
- Congenital ptosis of upper eyelidC0266573
- Eyelid ptosis congenitalC0266573
- Ptosis, congenitalC0266573
- congenital ptosisC0266573
- eyelid congenital upper ptosisC0266573
- ptosis congenitalC0266573
Clinical Terms
- Lower lacrimal punctum finding
- eyelid congenital upper ptosis
- Ectopia pupillae
- Bilateral congenital ptosis of upper eyelids
- Ectopic pupil
- Epicanthic fold
- Congenital ptosis of eyelid
- Congenital ptosis of left upper eyelid
- Blepharophimosis epicanthus inversus ptosis syndrome
- Congenital ptosis of upper eyelid
- Aniridia, ptosis, intellectual disability, familial obesity syndrome
- Ptosis, congenital
- Ptosis and vocal cord paralysis syndrome
- Aniridia
- Congenital absence of iris
- Recurrent laryngeal nerve palsy
- Congenital absence of lacrimal drainage structure
- Congenital aniridia
- Ohdo blepharophimosis syndrome
- Frydman Cohen Karmon syndrome
- Vagus nerve laryngeal paralysis
- Ectopia lentis
- Partial ablepharon
- Agenesis of iris
- Microbrachycephaly, ptosis, cleft lip syndrome
- Lower lacrimal punctum observation
- Open eye
- Faulk Epstein Jones syndrome
- Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
- ptosis congenital
- Deletion of part of long arm of chromosome 3
- Myogenic blepharoptosis
- BPES (blepharophimosis epicanthus inversus ptosis syndrome) plus
- Congenital dysgenetic ptosis
- Blepharophimosis epicanthus inversus ptosis syndrome plus
- Jackson Barr syndrome
- Irideraemia
- Ptosis of both upper eyelids
- 3q23 microdeletion syndrome
- Tucker syndrome
- Epicanthal fold
- Bilateral ptosis of upper eyelids
- Blepharoptosis, myopia, ectopia lentis syndrome
- Congenital ectopic lens
- Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
- Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome
- Eyelid ptosis congenital
- Corectopia
- BPES - blepharophimosis epicanthus inversus ptosis syndrome
- Ablepharon - absent eyelids
- Congenital Eyelid Ptosis
- McPherson Hall syndrome
- Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome
- Conductive deafness, ptosis, skeletal anomalies syndrome
- Congenital myogenic blepharoptosis
- Congenital subluxation of lens
- Congenital ptosis of both upper eyelids
- Myogenic ptosis
- Aplasia of iris
- Ablepharia
- Congenital ptosis of right upper eyelid
- Epicanthus inversus
- Irideremia
- Ablepharon
- Congenital ptosis of bilateral upper eyelids
- Dysgenesis of lacrimal punctum
- Blepharophimosis, intellectual disability syndrome
- Congenital drooping upper eyelid
- Congenital ectopic pupil
- Congenital ptosis (disorder)
- Richieri Costa Guion Almeida Ramos syndrome
- Congenital myogenic ptosis
- Metopic ridging, ptosis, facial dysmorphism syndrome
- Ptosis, strabismus, ectopic pupil syndrome
- Ptosis of bilateral upper eyelids
- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital ptosis?
The ICD-10-CM code for congenital ptosis is Q10.0. The full clinical description is "Congenital ptosis". Q10.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q10.0 mean?
ICD-10-CM code Q10.0 represents “Congenital ptosis”. 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 Q10.0 a billable code?
Yes, Q10.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q10.0 in?
Q10.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q10.0?
Q10.0 has Excludes1 notes indicating codes that cannot be used together with it, including: cryptophthalmos NOS (Q11.2); cryptophthalmos syndrome (Q87.0).
What SNOMED CT codes does Q10.0 map to?
Q10.0 maps to 35 SNOMED CT concepts: 890180006, 13401001, 69278003, 720987001, 715391004, and 30 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q10.0?
Q10.0 is linked to 1 UMLS Concept Unique Identifier: C0266573. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q10.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital ptosis 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 Q10.0?
Q10.0 maps to the ICD-11 code: LA14.04 (Congenital ptosis).
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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.