Congenital malformations of posterior segment of eye (Q14)
Clinical Information
Persistent Hyperplastic Primary Vitreous - A developmental ocular anomaly in which the primary VITREOUS BODY and its surrounding hyaloid vasculature failed to regress. It is usually unilateral and characterized by CATARACT; MICROPHTHALMOS (small eyeballs), and retrolenticular fibrovascular tissue. (from Yanoff: Ophthalmology, 2nd ed.)
Retinal Dysplasia - Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
Instructional Notations
Type 2 Excludes
A type 2 excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
- optic nerve hypoplasia H47.03
Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
Congenital malformations of eye, ear, face and neck (Q10-Q18)
Q14 Congenital malformations of posterior segment of eye
- Q14.0 Congenital malformation of vitreous humor
- Q14.1 Congenital malformation of retina
- Q14.2 Congenital malformation of optic disc
- Q14.3 Congenital malformation of choroid
- Q14.8 Other congenital malformations of posterior segment of eye
- Q14.9 Congenital malformation of posterior segment of eye, unspecified
Congenital malformations of posterior segment of eye (Q14)