ICD-11 code : LA12.3;
Preferred Label : Spherophakia;
ICD-11 definition : A disease of the eye, caused by homozygous mutations in the LTBP2 gene (isolated spherophakia),
or by other genetic mutations. This disease is characterised by small, spherical lenses.
This disease can also present with lenticular myopia, glaucoma, or sublation of the
lens into the vitreous cavity.;
ICD-11 synonym : congenital spherophakia;
ICD-11 inclusion : microspherophakia;
Origin ID : 1194029577;
UMLS CUI : C0266542;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- ICD-10 Mapping
- Semantic type(s)
- UMLS correspondences (same concept)
A disease of the eye, caused by homozygous mutations in the LTBP2 gene (isolated spherophakia),
or by other genetic mutations. This disease is characterised by small, spherical lenses.
This disease can also present with lenticular myopia, glaucoma, or sublation of the
lens into the vitreous cavity.
