All terms in MONDO
| Label | Id | Description |
|---|---|---|
| acetyl-CoA acetyltransferase-2 deficiency | MONDO_0013548 | |
| atrial fibrillation, familial, 12 | MONDO_0013545 | |
| mitochondrial complex V (ATP synthase) deficiency nuclear type 2 | MONDO_0013546 | |
| porcine postweaning multisystemic wasting syndrome | MONDO_0025506 | |
| perineocele | MONDO_0001559 | |
| deafness-lymphedema-leukemia syndrome | MONDO_0013540 | |
| pythiosis | MONDO_0025510 | |
| abnormal retinal correspondence | MONDO_0001565 | |
| binocular vision disease | MONDO_0001564 | |
| type II hypersensitivity reaction disease | MONDO_0025512 | |
| displacement of cardia through esophageal hiatus | MONDO_0001562 | |
| livedoid vasculopathy | MONDO_0025514 | |
| acoustic neuroma | MONDO_0001569 | |
| mixed receptive-expressive language disorder | MONDO_0001568 | |
| autoimmune urticaria | MONDO_0025513 | |
| obsolete alpha-2-macroglobulin deficiency | MONDO_0013538 | |
| hypotonia-failure to thrive-microcephaly syndrome | MONDO_0013539 | |
| pyloric stenosis | MONDO_0001561 | |
| psoriasis 13, susceptibility to | MONDO_0013554 | |
| Hermansky-Pudlak syndrome 3 | MONDO_0013555 |