Q10 |
Congenital malformations of eyelid, lacrimal apparatus and orbit [+]
Excludes 1: |
cryptophthalmos NOS (Q11.2) cryptophthalmos syndrome (Q87.0)
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Q10.0 |
Congenital ptosis
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Q10.1 |
Congenital ectropion
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Q10.2 |
Congenital entropion
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Q10.3 |
Other congenital malformations of eyelid Ablepharon Blepharophimosis, congenital Coloboma of eyelid Congenital absence or agenesis of cilia Congenital absence or agenesis of eyelid Congenital accessory eyelid Congenital accessory eye muscle Congenital malformation of eyelid NOS
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Q10.4 |
Absence and agenesis of lacrimal apparatus Congenital absence of punctum lacrimale
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Q10.5 |
Congenital stenosis and stricture of lacrimal duct
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Q10.6 |
Other congenital malformations of lacrimal apparatus Congenital malformation of lacrimal apparatus NOS
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Q10.7 |
Congenital malformation of orbit
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Q11 |
Anophthalmos, microphthalmos and macrophthalmos [+]
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Q11.0 |
Cystic eyeball
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Q11.1 |
Other anophthalmos Anophthalmos NOS Agenesis of eye Aplasia of eye
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Q11.2 |
Microphthalmos Cryptophthalmos NOS Dysplasia of eye Hypoplasia of eye Rudimentary eye
Excludes 1: |
cryptophthalmos syndrome (Q87.0)
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Q11.3 |
Macrophthalmos
Excludes 1: |
macrophthalmos in congenital glaucoma (Q15.0)
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Q12 |
Congenital lens malformations [+]
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Q12.0 |
Congenital cataract
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Q12.1 |
Congenital displaced lens
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Q12.2 |
Coloboma of lens
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Q12.3 |
Congenital aphakia
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Q12.4 |
Spherophakia
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Q12.8 |
Other congenital lens malformations Microphakia
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Q12.9 |
Congenital lens malformation, unspecified
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Q13 |
Congenital malformations of anterior segment of eye [+]
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Q13.0 |
Coloboma of iris Coloboma NOS
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Q13.1 |
Absence of iris Aniridia
Use additional |
code for associated glaucoma (H42) |
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Q13.2 |
Other congenital malformations of iris Anisocoria, congenital Atresia of pupil Congenital malformation of iris NOS Corectopia
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Q13.3 |
Congenital corneal opacity
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Q13.4 |
Other congenital corneal malformations Congenital malformation of cornea NOS Microcornea Peter's anomaly
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Q13.5 |
Blue sclera
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Q13.8 |
Other congenital malformations of anterior segment of eye [+]
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Q13.81 |
Rieger anomaly Axenfeld-Rieger syndrome
Code also |
any other associated congenital malformations such as cardiac defects
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Use additional |
code for associated glaucoma (H42) |
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Q13.89 |
Other congenital malformations of anterior segment of eye
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Q13.9 |
Congenital malformation of anterior segment of eye, unspecified
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Q14 |
Congenital malformations of posterior segment of eye [+]
Excludes 2: |
optic nerve hypoplasia (H47.03-)
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Q14.0 |
Congenital malformation of vitreous humor Congenital vitreous opacity
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Q14.1 |
Congenital malformation of retina Congenital retinal aneurysm
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Q14.2 |
Congenital malformation of optic disc Coloboma of optic disc
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Q14.3 |
Congenital malformation of choroid
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Q14.8 |
Other congenital malformations of posterior segment of eye Coloboma of the fundus
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Q14.9 |
Congenital malformation of posterior segment of eye, unspecified
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Q15 |
Other congenital malformations of eye [+]
Excludes 1: |
congenital nystagmus (H55.01) ocular albinism (E70.31-) optic nerve hypoplasia (H47.03-) retinitis pigmentosa (H35.52)
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Q15.0 |
Congenital glaucoma Axenfeld's anomaly Buphthalmos Glaucoma of childhood Glaucoma of newborn Hydrophthalmos Keratoglobus, congenital, with glaucoma Macrocornea with glaucoma Macrophthalmos in congenital glaucoma Megalocornea with glaucoma
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Q15.8 |
Other specified congenital malformations of eye
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Q15.9 |
Congenital malformation of eye, unspecified Congenital anomaly of eye Congenital deformity of eye
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Q16 |
Congenital malformations of ear causing impairment of hearing [+]
Excludes 1: |
congenital deafness (H90.-)
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Q16.0 |
Congenital absence of (ear) auricle
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Q16.1 |
Congenital absence, atresia and stricture of auditory canal (external) Congenital atresia or stricture of osseous meatus
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Q16.2 |
Absence of eustachian tube
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Q16.3 |
Congenital malformation of ear ossicles Congenital fusion of ear ossicles
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Q16.4 |
Other congenital malformations of middle ear Congenital malformation of middle ear NOS
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Q16.5 |
Congenital malformation of inner ear Congenital anomaly of membranous labyrinth Congenital anomaly of organ of Corti
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Q16.9 |
Congenital malformation of ear causing impairment of hearing, unspecified Congenital absence of ear NOS
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Q17 |
Other congenital malformations of ear [+]
Excludes 1: |
congenital malformations of ear with impairment of hearing (Q16.0-Q16.9) preauricular sinus (Q18.1)
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Q17.0 |
Accessory auricle Accessory tragus Polyotia Preauricular appendage or tag Supernumerary ear Supernumerary lobule
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Q17.1 |
Macrotia
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Q17.2 |
Microtia
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Q17.3 |
Other misshapen ear Pointed ear
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Q17.4 |
Misplaced ear Low-set ears
Excludes 1: |
cervical auricle (Q18.2)
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Q17.5 |
Prominent ear Bat ear
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Q17.8 |
Other specified congenital malformations of ear Congenital absence of lobe of ear
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Q17.9 |
Congenital malformation of ear, unspecified Congenital anomaly of ear NOS
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Q18 |
Other congenital malformations of face and neck [+]
Excludes 1: |
cleft lip and cleft palate (Q35-Q37) conditions classified to Q67.0-Q67.4 congenital malformations of skull and face bones (Q75.-) cyclopia (Q87.0) dentofacial anomalies [including malocclusion] (M26.-) malformation syndromes affecting facial appearance (Q87.0) persistent thyroglossal duct (Q89.2)
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Q18.0 |
Sinus, fistula and cyst of branchial cleft Branchial vestige
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Q18.1 |
Preauricular sinus and cyst Fistula of auricle, congenital Cervicoaural fistula
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Q18.2 |
Other branchial cleft malformations Branchial cleft malformation NOS Cervical auricle Otocephaly
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Q18.3 |
Webbing of neck Pterygium colli
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Q18.4 |
Macrostomia
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Q18.5 |
Microstomia
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Q18.6 |
Macrocheilia Hypertrophy of lip, congenital
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Q18.7 |
Microcheilia
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Q18.8 |
Other specified congenital malformations of face and neck Medial cyst of face and neck Medial fistula of face and neck Medial sinus of face and neck
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Q18.9 |
Congenital malformation of face and neck, unspecified Congenital anomaly NOS of face and neck
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