| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Pachyonychia congenita | MONDO:0016471 | 4 | |
| Striate palmoplantar keratoderma | MONDO:0018865 | 2 | |
| Focal palmoplantar and gingival keratoderma | MONDO:0007860 | ||
| Focal palmoplantar keratoderma with joint keratoses | MONDO:0018252 | ||
| Hereditary painful callosities | MONDO:0007248 | ||
| Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome | MONDO:0011884 | ||
| Isolated focal non-epidermolytic palmoplantar keratoderma | MONDO:0014622 | TRPV3 | |
| Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome | MONDO:0014460 | GRHL2 | |
| Palmoplantar keratoderma, nonepidermolytic, focal 1 | MONDO:0013073 | KRT16 | |
| Palmoplantar keratoderma-esophageal carcinoma syndrome | MONDO:0007856 | RHBDF2 | |
| Tyrosinemia type II | MONDO:0010160 | TAT | |
| Wooly hair-palmoplantar keratoderma syndrome | MONDO:0014492 | KANK2 |
Rare disease
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