1 => The disorder is placed on the map based on its association with a gene, but the underlying defect is not known
2 => The disorder has been placed on the map by linkage; no mutation has been found
3 => The molecular basis for the disorder is known; a mutation has been found in the gene
4 => A contiguous gene deletion or duplication syndrome, multiple genes are deleted or duplicated causing the phenotype
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| ICK | 6p12.1 | 612325 | R, REc | Endocrine-cerebroosteodysplasia, 612651 (3) | 612651 | 3 |
| ICK | 6p12.1 | 612325 | R, REc | {Epilepsy, juvenile myoclonic, susceptibility to, 10}, 617924 (3) | 617924 | 3 |