All terms in MONDO
| Label | Id | Description |
|---|---|---|
| ACTL6A-related BAFopathy | MONDO_0700121 | |
| SMARCC1-related BAFopathy | MONDO_0700123 | |
| PBRM1-related BAFopathy | MONDO_0700122 | |
| proximal chromosome 18q deletion syndrome | MONDO_0700118 | |
| chromosome 18q deletion syndrome | MONDO_0011147 | |
| distal chromosome 18q deletion syndrome | MONDO_0700119 | |
| microcephaly with lissencephaly and/or hydranencephaly | MONDO_0700116 | |
| pneumonia, non-human animal | MONDO_0700110 | |
| heterotaxy, visceral, 5, autosomal | MONDO_0700112 | |
| bacterial pneumonia, non-human animal | MONDO_0700111 | |
| Landau-Kleffner syndrome | MONDO_0009509 | |
| Lambotte syndrome | MONDO_0009508 | |
| Lambert syndrome | MONDO_0009507 | |
| specific granule deficiency | MONDO_0009506 | |
| lactic aciduria due to D-lactic acid | MONDO_0009505 | |
| mitochondrial DNA depletion syndrome 9 | MONDO_0009504 | |
| pyruvate dehydrogenase E3-binding protein deficiency | MONDO_0009503 | |
| pyruvate dehydrogenase E2 deficiency | MONDO_0009502 | |
| metabolic myopathy due to lactate transporter defect | MONDO_0009501 | |
| kuru, susceptibility to | MONDO_0009500 |