| Label | Id | |
|---|---|---|
| lattice corneal dystrophy, gelsolin type | C000657784 | |
| lattice corneal dystrophy, type II | C000657784 | |
| familial amyloidosis, finnish type | C000657784 | |
| syndrome associated with hypothyroidism | 15778 | |
| juvenile, aipl1-related retinitis pigmentosa | C565778 |