Template:ICD-11 Vision anomalies header table
|ICD-11 Structural developmental anomalies of the eye, eyelid or lacrimal apparatus|
LA10.0 Microphthalmos - This is a developmental disorder of the eye that literally means small eye (micros = small; ophthalmos = eye). One (Unilateral Microphthalmia) or both (Bilateral Microphthalmia) eyes may be involved.
LA10.1 Clinical anophthalmos - This refers to the clinical absence of one or both eyes. Both the globe (human eye) and the ocular tissue are missing from the orbit. The absence of the eye will cause a small bony orbit, a constricted mucosal socket, short eyelids, reduced palpebral fissure and malar prominence. Genetic mutations, chromosomal abnormalities, and prenatal environment can all cause anophthalmia. Anophthalmia is an extremely rare disease and is mostly rooted in genetic abnormalities.
LA10.3 Congenital macrophthalmos - A condition caused by failure of the eye to develop correctly during the antenatal period. This condition is characterized by enlargement of the globe of the eye.
LA12 Structural developmental anomalies of lens or zonula - LA12.0 Coloboma of lens LA12.1 Congenital cataract LA12.2 Congenital aphakia LA12.3 Spherophakia
LA13 Structural developmental anomalies of the posterior segment of eye - LA13.0 Congenital anomalies of the vitreous LA13.1 Coloboma of choroid or retina LA13.2 Coloboma of macula LA13.3 Congenital vitreoretinal dysplasia LA13.4 Optic pit LA13.5 Congenital retinal aneurysm LA13.6 Congenital malformations of choroid LA13.7 Congenital malformation of optic disc