All terms in MONDO
| Label | Id | Description |
|---|---|---|
| benign familial mesial temporal lobe epilepsy | MONDO_0015586 | |
| nephrosis | MONDO_0002331 | |
| hyperinsulinism due to HNF4A deficiency | MONDO_0016988 | |
| pachyonychia congenita 4 | MONDO_0014325 | |
| pachyonychia congenita 3 | MONDO_0014324 | |
| Fuchs heterochromic iridocyclitis | MONDO_0016989 | |
| retinitis pigmentosa 68 | MONDO_0014323 | |
| premature ovarian failure 9 | MONDO_0014322 | |
| gonococcal infection of joint | MONDO_0041903 | |
| atrial standstill 2 | MONDO_0014329 | |
| atrial standstill | MONDO_0015281 | |
| nevus of Ota | MONDO_0016984 | |
| developmental and epileptic encephalopathy, 19 | MONDO_0014328 | |
| nevus of Ito | MONDO_0016985 | |
| palmoplantar keratoderma, nonepidermolytic, focal or diffuse | MONDO_0014327 | |
| hereditary palmoplantar keratoderma | MONDO_0019272 | |
| congenital smooth muscle hamartoma | MONDO_0016986 | |
| nemaline myopathy 9 | MONDO_0014326 | |
| ATR-X-related syndrome | MONDO_0016980 | |
| infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome | MONDO_0016981 |