All terms in MONDO
| Label | Id | Description |
|---|---|---|
| blood group incompatibility | MONDO_0002901 | |
| retinal vasculitis | MONDO_0006950 | |
| retinitis | MONDO_0002708 | |
| medial condensing osteitis of the clavicle | MONDO_0018929 | |
| obsolete rare hepatic disease | MONDO_0018928 | |
| centronuclear myopathy | MONDO_0018947 | |
| rhombencephalosynapsis | MONDO_0018946 | |
| cerebellar malformation | MONDO_0015915 | |
| pneumonitis | MONDO_0043905 | |
| distal myopathy | MONDO_0018949 | |
| leishmaniasis, diffuse cutaneous | MONDO_0043904 | |
| cutaneous leishmaniasis | MONDO_0005446 | |
| multiminicore myopathy | MONDO_0018948 | |
| congenital myopathy with cores | MONDO_0015765 | |
| qualitative or quantitative defects of selenoprotein N1 | MONDO_0016197 | |
| congenital structural myopathy | MONDO_0002921 | |
| macrophagic myofasciitis | MONDO_0018942 | |
| acquired skeletal muscle disease | MONDO_0016105 | |
| McLeod neuroacanthocytosis syndrome | MONDO_0018945 | |
| furuncular myiasis | MONDO_0018941 |