All terms in MONDO
| Label | Id | Description |
|---|---|---|
| obsolete Brooks-Wisniewski-brown syndrome | MONDO_0010376 | |
| hyperbilirubinemia, shunt, primary | MONDO_0009382 | |
| developmental and epileptic encephalopathy, 8 | MONDO_0010375 | |
| hereditary hyperekplexia | MONDO_0021022 | |
| hyperbilirubinemia, conjugated, type 3 | MONDO_0009381 | |
| X-linked hereditary sensory and autonomic neuropathy with hearing loss | MONDO_0010378 | |
| Dubin-Johnson syndrome | MONDO_0009380 | |
| myopia 13, X-linked | MONDO_0010377 | |
| Brunner syndrome | MONDO_0010379 | |
| ALK+ histiocytosis | MONDO_0022338 | |
| Cornelia de Lange syndrome 2 | MONDO_0010370 | |
| obsolete Clark-Baraitser syndrome | MONDO_0010372 | |
| Aland island eye disease | MONDO_0010371 | |
| hyperlysinemia due to defect in lysine transport into mitochondria | MONDO_0009389 | |
| hyperlysinemia | MONDO_0009388 | |
| familial lipoprotein lipase deficiency | MONDO_0009387 | |
| hyperlipoproteinemia | MONDO_0037748 | |
| hyperlexia | MONDO_0009386 | |
| reading disorder | MONDO_0001697 | |
| hyperparathyroidism, neonatal self-limited primary, with hypercalciuria | MONDO_0009396 |