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 |
| KRT8 | 12q13.13 | 148060 | Psh | Cirrhosis, cryptogenic, 215600 (3) | 215600 | 3 |
| KRT8 | 12q13.13 | 148060 | Psh | {Cirrhosis, noncryptogenic, susceptibility to}, 215600 (3) | 215600 | 3 |