Q10.0
BillableCongenital ptosis
Congenital ptosis
Status
Billable / Specific
Parent Code
Q10Coding 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 metabolism (E70-E88)
- cleft lip and cleft palate (Q35-Q37)
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- congenital malformation of larynx (Q31.-)
- congenital malformation of lip NEC (Q38.0)
- congenital malformation of nose (Q30.-)
- congenital malformation of parathyroid gland (Q89.2)
- congenital malformation of thyroid gland (Q89.2)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code Q10.0?
ICD-10-CM code Q10.0 represents "Congenital ptosis". It 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.
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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.