All terms in MONDO
| Label | Id | Description |
|---|---|---|
| post-infectious syndrome | MONDO_0021670 | |
| left ventricular noncompaction 5 | MONDO_0800351 | |
| mosaic trisomy 6 | MONDO_0043277 | |
| chromosome 6 disorder | MONDO_0700013 | |
| mosaic | MONDO_0700062 | |
| obsolete rhegmatogenous retinal detachment, autosomal dominant | MONDO_0800343 | |
| brachydactyly-syndactyly-oligodactyly syndrome | MONDO_0800344 | |
| skeletal system disorder | MONDO_0005172 | |
| congenital myopathy 4A, autosomal dominant | MONDO_0800341 | |
| cap myopathy | MONDO_0015753 | |
| cap myopathy 2 | MONDO_0800342 | |
| cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction | MONDO_0800347 | |
| familial hypertrophic cardiomyopathy | MONDO_0024573 | |
| retinitis pigmentosa 53 | MONDO_0800348 | |
| atrial fibrillation, familial, 17 | MONDO_0800345 | |
| familial atrial fibrillation | MONDO_0018054 | |
| left ventricular noncompaction 9 | MONDO_0800346 | |
| atrial fibrillation, familial, 16 | MONDO_0800349 | |
| silicosiderosis | MONDO_0043283 | |
| silicosis | MONDO_0005960 |