Mapped loci for human congenital non-syndromic cataract with no candidate gene. Evidence for linkage to each locus is based upon the publication of single family data
| Phenotype | Locus | Inheritance | OMIM No | Reference |
| Volkmann (pulverulent) | 1p36 | Autosomal dominant | 115665 | 67 |
| Posterior polar | 1p36 | Autosomal dominant | 116600 | 25 |
| Anterior polar | 14q24 | Translocation | 115650 | 24 |
| Unknown | 16p13.3 | Translocation | 156850 | 60 |
| Marner | 16q22.1 | Autosomal dominant | 116800 | 57 |
| Posterior polar | 16q22.1 | Autosomal dominant | 116800 | 57 |
| Anterior polar | 17p13 | Autosomal dominant | 601202 | 26 |
| Zonular-sutural (lamellar) | 17q11-12 | Autosomal dominant | 600881 | 55 |
| Cerulean | 17q24 | Autosomal dominant | 115660 | 58 |
| Unknown | I blood group locus | Autosomal recessive | 212500 | 68 |
| Sutural (lamellar) | Xpter-Xqter | X linked recessive | 302200 | 69 |
| (possibly synonymous with Nance-Horan syndrome) | (the recognition of various deletions probably refine the region to Xp22.3-21.138 70) |
OMIM refers to Online Mendelian Inheritance in Man (http://www3.ncbi.nih.gov/Omim/searchomain.html)