Interval Showing the Linkage Disequilibrium in the Disease Alleles of Finnish Disease Heritage
| Disease | Gene location | Interval (cM) |
| Autoimmune polyendocrinopathy–candidiasis– ectodermal dystrophy (APECED) | 21q22.3 | 3 |
| Cartilage-hair hypoplasia (CHH) | 9p21–p13 | 3 |
| Choroideremia | Xq21 | 9 |
| Congenital chloride diarrhoea (CCD) | 7q31 | 13 |
| Congenital nephrosis (CNF) | 19q12–q13.1 | 3 |
| Cornea plana congenita | 12q21 | 2.5 |
| Diastrophic dysplasia (DTD) | 5q31–q34 | 2 |
| Familial amyloidosis, Finnish type (FAF) | 9q33 | 3.5 |
| Infantile neuronal ceroid-lipofuscinosis (INCL) | 1p32 | 2.5 |
| Infantile onset spinocerebellar ataxia (IOSCA) | 10q23.3–q24.1 | 5 |
| Northern epilepsy (Kainuu epilepsy) | 8ptel. | 10 |
| Progressive myoclonus epilepsy (PME) | 21q22 | 5 |
| Retinoschisis | Xp22.2–p22.1 | 10 |
| Salladisease | 6q14–q15 | 10 |
| Usher syndrome, type III (USH3) | 3q21–q25 | 7.5 |
| Variant form of late infantile NCL (vLINCL) | 13q21.1–q32 | 11 |
[i] For original references, see Peltonen et al. (1995).